FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1995348626> ?p ?o ?g. }

• W1995348626 endingPage "1614" @default.
• W1995348626 startingPage "1607" @default.
• W1995348626 abstract "The homeodomain transcription factor Nkx3.1 and the cyclin-dependent kinase inhibitor p27kip1 have both been implicated in prostate tumor suppression. In addition, both of these molecules demonstrate haploinsufficiency for tumor suppression, in which loss of a single allele is sufficient to lead to the development of preneoplastic or neoplastic lesions. We have generated mice carrying compound mutant alleles of Nkx3.1 and p27 to explore the roles of these factors in prostate tumorigenesis. Our results indicate that Nkx3.1 and p27kip1 cooperate to suppress the proliferation of prostatic epithelial cells and the formation of preneoplastic lesions resembling prostatic intraepithelial neoplasia. Cooperativity was most evident with complete loss of at least one of the two genes because compound heterozygous mice exhibited a prostatic phenotype that was no more severe than that of single heterozygous mutants. Thus Nkx3.1 and p27kip1 regulate prostatic epithelial cell proliferation and tumor initiation by affecting both haploinsufficient and nonhaploinsufficient pathways. The homeodomain transcription factor Nkx3.1 and the cyclin-dependent kinase inhibitor p27kip1 have both been implicated in prostate tumor suppression. In addition, both of these molecules demonstrate haploinsufficiency for tumor suppression, in which loss of a single allele is sufficient to lead to the development of preneoplastic or neoplastic lesions. We have generated mice carrying compound mutant alleles of Nkx3.1 and p27 to explore the roles of these factors in prostate tumorigenesis. Our results indicate that Nkx3.1 and p27kip1 cooperate to suppress the proliferation of prostatic epithelial cells and the formation of preneoplastic lesions resembling prostatic intraepithelial neoplasia. Cooperativity was most evident with complete loss of at least one of the two genes because compound heterozygous mice exhibited a prostatic phenotype that was no more severe than that of single heterozygous mutants. Thus Nkx3.1 and p27kip1 regulate prostatic epithelial cell proliferation and tumor initiation by affecting both haploinsufficient and nonhaploinsufficient pathways. Prostate tumor development is contingent on the accumulation of mutations in multiple oncogenes and tumor suppressor genes. Recent human and transgenic mouse model studies have established roles for two tumor suppressor genes, the homeodomain transcription factor Nkx3.1 and the cyclin-dependent kinase inhibitor p27kip1 in prostate tumorigenesis. The NKX3.1 gene is localized to human chromosome 8p21, a region that undergoes loss of heterozygosity with high frequency in prostate cancers and prostatic intraepithelial neoplasia (PIN) lesions.1Emmert-Buck MR Vocke CD Pozzatti RO Duray PH Jennings SB Florence CD Zhuang Z Bostwick DG Liotta LA Linehan WM Allelic loss on chromosome 8p12-21 in microdissected prostatic intraepithelial neoplasia.Cancer Res. 1995; 55: 2959-2962PubMed Google Scholar, 2He WW Sciavolino PJ Wing J Augustus M Hudson P Meissner PS Curtis RT Shell BK Bostwick DG Tindall DJ Gelmann EP Abate-Shen C Carter KC A novel human prostate-specific, androgen-regulated homeobox gene (NKX3.1) that maps to 8p21, a region frequently deleted in prostate cancer.Genomics. 1997; 43: 69-77Crossref PubMed Scopus (297) Google Scholar Evidence that NKX3.1 is a relevant prostate tumor suppressor gene targeted by loss of heterozygosity at 8p21 has come from studies that show loss of NKX3.1 protein expression in a majority of human prostate tumors.3Bowen C Bubendorf L Voeller HJ Slack R Willi N Sauter G Gasser TC Koivisto P Lack EE Kononen J Kallioniemi OP Gelmann EP Loss of NKX3.1 expression in human prostate cancers correlates with tumor progression.Cancer Res. 2000; 60: 6111-6115PubMed Google Scholar, 4Kim MJ Bhatia-Gaur R Banach-Petrosky WA Desai N Wang Y Hayward SW Cunha GR Cardiff RD Shen MM Abate-Shen C Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis.Cancer Res. 2002; 62: 2999-3004PubMed Google Scholar Loss of NKX3.1 protein expression is also significantly correlated with tumor progression.3Bowen C Bubendorf L Voeller HJ Slack R Willi N Sauter G Gasser TC Koivisto P Lack EE Kononen J Kallioniemi OP Gelmann EP Loss of NKX3.1 expression in human prostate cancers correlates with tumor progression.Cancer Res. 2000; 60: 6111-6115PubMed Google Scholar Mice with deletion of one or both alleles of Nkx3.1 develop prostatic epithelial hyperplasia and PIN4Kim MJ Bhatia-Gaur R Banach-Petrosky WA Desai N Wang Y Hayward SW Cunha GR Cardiff RD Shen MM Abate-Shen C Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis.Cancer Res. 2002; 62: 2999-3004PubMed Google Scholar, 5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 6Bhatia-Gaur R Donjacour AA Sciavolino PJ Kim M Desai N Young P Norton CR Gridley T Cardiff RD Cunha GR Abate-Shen C Shen MM Roles for Nkx3.1 in prostate development and cancer.Genes Dev. 1999; 13: 966-977Crossref PubMed Scopus (517) Google Scholar indicating that Nkx3.1 functions as an haploinsufficient tumor suppressor gene. Recent evidence indicates that Nkx3.1 regulates the exit of regenerating prostatic epithelial cells from the cell cycle in a dosage-sensitive manner, thereby leading to hyperplasia.7Magee JA Abdulkadir SA Milbrandt J Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation.Cancer Cell. 2003; 3: 273-283Abstract Full Text Full Text PDF PubMed Scopus (117) Google Scholar Furthermore, in mice, loss of Nkx3.1 cooperates with loss of the tumor suppressor, Pten, to promote prostate tumorigenesis.8Kim MJ Cardiff RD Desai N Banach-Petrosky WA Parsons R Shen MM Abate-Shen C Cooperativity of Nkx3.1 and Pten loss of function in a mouse model of prostate carcinogenesis.Proc Natl Acad Sci USA. 2002; 99: 2884-2889Crossref PubMed Scopus (260) Google Scholar Similar to NKX3.1, expression of the cyclin-dependent kinase inhibitor p27KIP1 is lost in a large fraction of human prostate carcinomas, and reduced or absent expression of p27KIP1 correlates with poor patient prognosis.9Macri E Loda M Role of p27 in prostate carcinogenesis.Cancer Metastasis Rev. 1998; 17: 337-344Crossref PubMed Scopus (67) Google Scholar Deletion of p27 in mice also results in prostatic epithelial hyperplasia and cooperates with loss of Pten to promote prostate tumor development.10Cordon-Cardo C Koff A Drobnjak M Capodieci P Osman I Millard SS Gaudin PB Fazzari M Zhang ZF Massague J Scher HI Distinct altered patterns of p27KIP1 gene expression in benign prostatic hyperplasia and prostatic carcinoma.J Natl Cancer Inst. 1998; 90: 1284-1291Crossref PubMed Scopus (242) Google Scholar, 11Di Cristofano A De Acetis M Koff A Cordon-Cardo C Pandolfi PP Pten and p27KIP1 cooperate in prostate cancer tumor suppression in the mouse.Nat Genet. 2001; 27: 222-224Crossref PubMed Scopus (398) Google Scholar Finally, p27kip1 also demonstrates haploinsufficiency for tumor suppression because loss of one p27 allele can be sufficient for expression of the tumorigenic phenotype.11Di Cristofano A De Acetis M Koff A Cordon-Cardo C Pandolfi PP Pten and p27KIP1 cooperate in prostate cancer tumor suppression in the mouse.Nat Genet. 2001; 27: 222-224Crossref PubMed Scopus (398) Google Scholar, 12Fero ML Randel E Gurley KE Roberts JM Kemp CJ The murine gene p27Kip1 is haplo-insufficient for tumour suppression.Nature. 1998; 396: 177-180Crossref PubMed Scopus (680) Google Scholar To examine the roles of Nkx3.1 and p27 in regulating prostate tumorigenesis in particular with regards to haploinsufficiency, we have generated and analyzed mice carrying all possible permutations of loss-of-function alleles of the two genes. Our results indicate cooperativity between Nkx3.1 and p27kip1 in suppressing epithelial proliferation and development of PIN lesions. Furthermore, these effects of Nkx3.1 and p27kip1 are mediated via both haploinsufficient and nonhaploinsufficient pathways. Nkx3.1 and p27 mutant mice have been described previously.5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 13Fero ML Rivkin M Tasch M Porter P Carow CE Firpo E Polyak K Tsai LH Broudy V Perlmutter RM Kaushansky K Roberts JM A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice.Cell. 1996; 85: 733-744Abstract Full Text Full Text PDF PubMed Scopus (1323) Google Scholar Mice were genotyped by polymerase chain reaction on tail DNA. Nkx3.1+/−p27+/− mice generated on a mixed C57BL6J/129Sv background were intercrossed to generate the compound mutant mice used for analyses (Table 1). Not all offspring from the matings were entered into the study. The urogenital tract, including prostate, seminal vesicles, and testes were harvested and fixed in 4% paraformaldehyde. Paraffin-embedded sections were stained with hematoxylin and eosin (H&E) and evaluated histologically by a blinded pathologist (IAE). Prostate pathology was scored according to the following histopathological grading scale, which is a modification of the score suggested by Park and colleagues.14Park JH Walls JE Galvez JJ Kim M Abate-Shen C Shen MM Cardiff RD Prostatic intraepithelial neoplasia in genetically engineered mice.Am J Pathol. 2002; 161: 727-735Abstract Full Text Full Text PDF PubMed Scopus (138) Google Scholar Normal, benign prostatic epithelium with normal nuclear morphology. Grade 1: Lesion demonstrating prostatic epithelial hyperplasia without atypia. Atypia here refers to the presence of nuclear crowding, nuclear elongation, and hyperchromasia. Grade 2: Lesion showing prostatic epithelial hyperplasia with mild atypia. Grade 3: Lesion showing prostatic epithelial hyperplasia with moderate atypia. Grade 4: Lesion showing prostatic epithelial hyperplasia with marked atypia.Table 1Number of Mice Generated and Sacrificed by Genotype and AgeAge (weeks)p+/+ n+/+p+/+ n+/−p+/+ n−/−p+/− n+/+p−/− n+/+p+/− n+/−p+/− n−/−p−/− n+/−p−/− n−/−Total128668215543572415441071911ND4743612861591610101096Total351816331850261417227ND, not done. Open table in a new tab ND, not done. Paraffin sections were stained using the Feulgen stain (Chroma Vision, San Juan Capistrano, CA). Nuclear images were extracted from the Feulgen-stained histological sections using the Cell Finder software and individual nuclei were analyzed using the Nuclear Grade software (Bacus Laboratories Inc.). Image morphometric nuclear grading was performed using the software as described.15Bacus JW Boone CW Bacus JV Follen M Kelloff GJ Kagan V Lippman SM Image morphometric nuclear grading of intraepithelial neoplastic lesions with applications to cancer chemoprevention trials.Cancer Epidemiol Biomarkers Prev. 1999; 8: 1087-1094PubMed Google Scholar Raw data of DNA mass and nuclear size were then imported into Excel spread sheet and then into SPSS statistical program. The control and the double-knockout groups were then compared using Student's t-test. Prostate extracts were subjected to Western blot analysis as described.16Yang S-Z Abdulkadir SA Early growth response gene 1 modulates androgen receptor signaling in prostate carcinoma cells.J Biol Chem. 2003; 278: 39906-39911Crossref PubMed Scopus (55) Google Scholar Primary antibodies used were polyclonal anti-Nkx3.1 antibody17Abdulkadir SA Carvalhal GF Kaleem Z Kisiel W Humphrey PA Catalona WJ Milbrandt J Tissue factor expression and angiogenesis in human prostate carcinoma.Hum Pathol. 2000; 31: 443-447Abstract Full Text PDF PubMed Scopus (131) Google Scholar at 1:20 dilution and polyclonal anti-p27kip1 antibody (1:1000, Santa Cruz). Immunohistochemical staining was performed using the high-temperature (microwave) antigen retrieval method as described.17Abdulkadir SA Carvalhal GF Kaleem Z Kisiel W Humphrey PA Catalona WJ Milbrandt J Tissue factor expression and angiogenesis in human prostate carcinoma.Hum Pathol. 2000; 31: 443-447Abstract Full Text PDF PubMed Scopus (131) Google Scholar, 18Abdulkadir SA Carbone JM Naughton CK Humphrey PA Catalona WJ Milbrandt J Frequent and early loss of the EGR1 corepressor NAB2 in human prostate carcinoma.Hum Pathol. 2001; 32: 935-939Abstract Full Text Full Text PDF PubMed Scopus (57) Google Scholar The following primary antibodies were used: rabbit polyclonal anti-Nkx3.1 antibody at 1:100 dilution,17Abdulkadir SA Carvalhal GF Kaleem Z Kisiel W Humphrey PA Catalona WJ Milbrandt J Tissue factor expression and angiogenesis in human prostate carcinoma.Hum Pathol. 2000; 31: 443-447Abstract Full Text PDF PubMed Scopus (131) Google Scholar rabbit polyclonal anti-p27kip1 (1:100, Santa Cruz), rabbit polyclonal anti-Ki67 antibody (1:1000, Novocastra) and mouse monoclonal anti-proliferating cell nuclear antigen (PCNA) antibody (1:200, Santa Cruz). Testes present on the same slide served as internal controls for Ki-67 and PCNA staining. Sections were developed using 3,3′-diaminobenzidine in Tris-buffered saline and 0.003% hydrogen peroxide, counterstained with hematoxylin, dehydrated, cleared, and mounted for viewing. For determination of the Ki-67- and PCNA-labeling indices, a minimum of 1000 cells were counted. All counts were done in the anterior lobes of the prostates for consistency. The TiterTACS kit (R&D Systems, Minneapolis, MN) was used according to the manufacturer's instructions for detection of apoptotic cells. Testes present on the same slide served as internal controls. A minimum of 1000 cells in the anterior lobes was counted for determination of the apoptotic index. Previous studies have shown that loss of either Nkx3.1 or p27 could cooperate with loss of the Pten tumor suppressor gene in mice to promote prostate tumorigenesis.8Kim MJ Cardiff RD Desai N Banach-Petrosky WA Parsons R Shen MM Abate-Shen C Cooperativity of Nkx3.1 and Pten loss of function in a mouse model of prostate carcinogenesis.Proc Natl Acad Sci USA. 2002; 99: 2884-2889Crossref PubMed Scopus (260) Google Scholar, 11Di Cristofano A De Acetis M Koff A Cordon-Cardo C Pandolfi PP Pten and p27KIP1 cooperate in prostate cancer tumor suppression in the mouse.Nat Genet. 2001; 27: 222-224Crossref PubMed Scopus (398) Google Scholar To determine whether loss of Nkx3.1 and loss of p27 cooperate in prostate tumorigenesis, we generated cohorts of compound mutant mice corresponding to the nine possible genotypes (Table 1). Using Western blot analyses, we determined that lack of Nkx3.1 does not significantly affect p27kip1 expression levels (Figure 1A). Conversely, loss of p27 also does not significantly alter Nkx3.1 levels (Figure 1B). The prostates of mutant animals were examined for histopathological abnormalities at various ages (12 weeks, 24 weeks, and 36 weeks). As reported previously4Kim MJ Bhatia-Gaur R Banach-Petrosky WA Desai N Wang Y Hayward SW Cunha GR Cardiff RD Shen MM Abate-Shen C Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis.Cancer Res. 2002; 62: 2999-3004PubMed Google Scholar, 5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 6Bhatia-Gaur R Donjacour AA Sciavolino PJ Kim M Desai N Young P Norton CR Gridley T Cardiff RD Cunha GR Abate-Shen C Shen MM Roles for Nkx3.1 in prostate development and cancer.Genes Dev. 1999; 13: 966-977Crossref PubMed Scopus (517) Google Scholar Nkx3.1−/− and Nkx3.1+/− mutant mice display prostatic epithelial hyperplasia and dysplasia (data not shown). Lesions were identified both in the anterior and dorsolateral lobes of the prostate, but they were more extensive in the anterior lobe. For consistency, all further analyses described herein were performed on the anterior prostate. p27−/− and p27+/− mice also show evidence of hyperplasia and dysplasia, which however, are generally less severe than that seen in Nkx3.1 mutant mice. Compound mutant mice, particularly p27−/−Nkx3.1−/−, p27−/−Nkx3.1+/−, and p27+/−Nkx3.1−/− animals showed more extensive lesions with increasing nuclear crowding, nuclear elongation, and hyperchromasia (Figure 2).Figure 2Prostate histopathology in p27 × Nkx3.1 compound mutant mice. Anterior prostates from 36-week-old mice were stained by H&E and examined histologically. A and B: Normal-looking prostate from a p27+/+Nkx3.1+/+ animal scored as grade 0. C to F: Prostatic lesions from p27−/−Nkx3/1−/− mice showing prostatic epithelial hyperplasia with atypia including marked nuclear crowding, nuclear elongation, and hyperchromasia. Original magnifications: ×20 (A, C); ×100 (B, D–F).View Large Image Figure ViewerDownload Hi-res image Download (PPT) We used a histopathological grading system in an attempt at objectively assessing the impact of loss of Nkx3.1 and p27 on prostatic pathology. Prostates are assigned scores from 0 to 4, with 0 representing normal looking epithelium and 4 representing the most severe lesions observed as detailed in the Materials and Methods section. As shown in Figure 3, complete loss of both alleles of Nkx3.1 and p27 leads to an increased incidence of PIN-like lesions (histopathological score 3 to 4). In this group (p27−/−Nkx3.1−/−), 100% of the animals have developed PIN-like lesions by 24 weeks of age. An increase in the incidence of PIN-like lesions was also observed in 36-week-old p27−/−Nkx3.1+/− and p27+/−Nkx3.1−/− mice (Figure 3). Histologically, the lesions in old p27−/−Nkx3.1+/− and p27+/−Nkx3.1−/− animals were indistinguishable from those in p27−/−Nkx3.1−/− mice. We were particularly interested in whether p27+/−Nkx3.1+/− compound heterozygous mice will show evidence of cooperativity, because both Nkx3.1 and p27 are reported to show haploinsufficiency for tumor suppression.4Kim MJ Bhatia-Gaur R Banach-Petrosky WA Desai N Wang Y Hayward SW Cunha GR Cardiff RD Shen MM Abate-Shen C Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis.Cancer Res. 2002; 62: 2999-3004PubMed Google Scholar, 5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 6Bhatia-Gaur R Donjacour AA Sciavolino PJ Kim M Desai N Young P Norton CR Gridley T Cardiff RD Cunha GR Abate-Shen C Shen MM Roles for Nkx3.1 in prostate development and cancer.Genes Dev. 1999; 13: 966-977Crossref PubMed Scopus (517) Google Scholar, 12Fero ML Randel E Gurley KE Roberts JM Kemp CJ The murine gene p27Kip1 is haplo-insufficient for tumour suppression.Nature. 1998; 396: 177-180Crossref PubMed Scopus (680) Google Scholar Analysis of p27+/−Nkx3.1+/− mice indicates no evidence for cooperativity in induction of PIN lesions in these animals (Figure 3) because the phenotype of p27+/−Nkx3.1+/− mice was no worse than that of p27+/−Nkx3.1+/+ or p27+/+Nkx3.1+/− mice at all ages examined. We further characterized the prostatic lesions in the mutant animals using morphometric analysis of Feulgen-stained nuclei. Using imaging software, nuclei were extracted from wild-type and p27−/−Nkx3.1−/− double-knockout animals. Nuclei from mutant animals were significantly larger and had higher DNA content (Figure 4), confirming their dysplastic nature as judged by standard histopathological examination. To ascertain the degree to which our histopathological grading score correlates with morphometric analysis of Feulgen-stained nuclei, we used the image morphometric nuclear grading method of Bacus and colleagues.15Bacus JW Boone CW Bacus JV Follen M Kelloff GJ Kagan V Lippman SM Image morphometric nuclear grading of intraepithelial neoplastic lesions with applications to cancer chemoprevention trials.Cancer Epidemiol Biomarkers Prev. 1999; 8: 1087-1094PubMed Google Scholar The imaging software uses multiple parameters, including nuclear area, DNA mass, pleomorphism, entropy, circularity, elongation, coarseness, and angularity to calculate the image morphometric nuclear grade score. The image morphometric nuclear grade correlated well with the histopathogical grading score determined by examination of H&E-stained sections (Figure 4E). We next examined the proliferative rates of prostate epithelial cells in the mutant mice using Ki67 staining. We have previously shown that Ki67 is a valid marker for, and correlates well with, DNA synthesis as measured by BrdU (bromodeoxyuridine) incorporation in mouse prostate epithelial cells.7Magee JA Abdulkadir SA Milbrandt J Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation.Cancer Cell. 2003; 3: 273-283Abstract Full Text Full Text PDF PubMed Scopus (117) Google Scholar Wild-type mouse prostate showed a low-Ki67-labeling index (Figure 5). Consistent with previous reports5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 6Bhatia-Gaur R Donjacour AA Sciavolino PJ Kim M Desai N Young P Norton CR Gridley T Cardiff RD Cunha GR Abate-Shen C Shen MM Roles for Nkx3.1 in prostate development and cancer.Genes Dev. 1999; 13: 966-977Crossref PubMed Scopus (517) Google Scholar, 7Magee JA Abdulkadir SA Milbrandt J Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation.Cancer Cell. 2003; 3: 273-283Abstract Full Text Full Text PDF PubMed Scopus (117) Google Scholar, 10Cordon-Cardo C Koff A Drobnjak M Capodieci P Osman I Millard SS Gaudin PB Fazzari M Zhang ZF Massague J Scher HI Distinct altered patterns of p27KIP1 gene expression in benign prostatic hyperplasia and prostatic carcinoma.J Natl Cancer Inst. 1998; 90: 1284-1291Crossref PubMed Scopus (242) Google Scholar loss of a single Nkx3.1 or p27 allele leads to a modest increase in Ki67 labeling (Figure 5). A further increase in Ki67-positive cells is seen when both alleles of either gene are lost (p27−/−Nkx3.1+/+ and p27+/+Nkx3.1−/−). Double-knockout mice have a significant increase in Ki67 labeling indicative of a synergistic effect between the two molecules in suppressing the proliferation of prostatic epithelial cells. Consistent with the results of our histopathological examination, the proliferative rates in compound heterozygous, p27+/−Nkx3.1+/− animals was the same as that in p27+/−Nkx3.1+/+ or p27+/+Nkx3.1+/− animals, indicating lack of cooperation when at least one allele of either gene is retained. Furthermore, the Ki67-labeling index of p27−/−Nkx3.1+/+ mice is not significantly different from that of p27−/−Nkx3.1+/− animals. Nor did the Ki67-labeling index of p27+/+Nkx3.1−/− animals differ significantly from that of p27+/−Nkx3.1−/− mice. These results were confirmed by performing a similar quantitative analysis using a different marker associated with proliferation, the PCNA (Figure 5F). We thus conclude that Nkx3.1 and p27 regulate the proliferation of prostate epithelial cells through both haploinsufficient and nonhaploinsufficient pathways. We used the TUNEL assay to examine apoptosis in the prostates of mutant mice. The apoptotic rate was low in the prostates of wild-type mice, and was not significantly altered in the prostates of p27+/+Nkx3.1+/−, p27+/+Nkx3.1−/−, p27+/−Nkx3.1+/+, p27+/−Nkx3.1−/−, or p27+/−Nkx3.1+/− animals (Figure 6). By contrast, the apoptotic rate was modestly but significantly increased in mutants lacking p27 and retaining at least one allele of Nkx3.1 (ie, p27−/−Nkx3.1+/+ and p27−/−Nkx3.1+/− mice, P ≤ 0.05). However, this increase was not apparent in double-knockout mice (p27−/−Nkx3.1−/−), despite the striking increase in proliferation seen in these animals (Figure 5). These results suggest that lack of p27 leads to an increase in apoptosis in the prostate, but this is suppressed in mice lacking Nkx3.1. Progression of prostatic epithelial hyperplasia to dysplasia is associated with loss of Nkx3.1 protein expression.5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 8Kim MJ Cardiff RD Desai N Banach-Petrosky WA Parsons R Shen MM Abate-Shen C Cooperativity of Nkx3.1 and Pten loss of function in a mouse model of prostate carcinogenesis.Proc Natl Acad Sci USA. 2002; 99: 2884-2889Crossref PubMed Scopus (260) Google Scholar We therefore examined lesions from p27-deficient mice for evidence of loss of Nkx3.1 protein expression. We found focal areas of loss of Nkx3.1 expression in lesions from p27−/−Nkx3.1+/− and p27−/−Nkx3.1+/+ mice (Figure 7). To determine whether p27kip1 expression is lost in Nkx3.1 mutant prostates, we examined the lesions of p27+/−Nkx3.1−/− and p27+/−Nkx3.1+/− animals. In contrast to wild-type prostates, which show a more uniform expression of p27kip1, the mutant prostates exhibit a more heterogeneous expression, with areas of focal loss of expression (Figure 7). Thus cells exist in foci of dysplastic cells in compound mutant mice where protein expression from the wild-type allele is silenced, effectively rendering the involved cells null for the protein in question (p27kip1 or Nkx3.1). In sum, these results support the notion that loss of Nkx3.1 and p27kip1 protein expression, which are observed in PIN lesions in human prostate carcinoma may have a role in promoting prostate tumor initiation. Details of the processes that regulate prostate cancer initiation remain poorly understood. Current evidence points to PIN as a precursor lesion for prostate cancer, yet the genetic and molecular changes required for benign prostate epithelial cells to develop into PIN are not fully understood. Recently, the prostate-specific homeodomain transcription factor NKX3.1 has emerged as a candidate tumor suppressor gene whose loss is associated with prostate tumor initiation.19Abate-Shen C Shen MM Molecular genetics of prostate cancer.Genes Dev. 2000; 14: 2410-2434Crossref PubMed Scopus (543) Google Scholar Re-expression of NKX3.1 in human prostate carcinoma cell lines negative for NKX3.1 results in suppression of growth and tumorigenicity, and deletion of Nkx3.1 in mice results in prostatic epithelial hyperplasia and PIN.4Kim MJ Bhatia-Gaur R Banach-Petrosky WA Desai N Wang Y Hayward SW Cunha GR Cardiff RD Shen MM Abate-Shen C Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis.Cancer Res. 2002; 62: 2999-3004PubMed Google Scholar, 5Abdulkadir SA Magee JA Peters TJ Kaleem Z Naughton CK Humphrey PA Milbrandt J Conditional loss of nkx3.1 in adult mice induces prostatic intraepithelial neoplasia.Mol Cell Biol. 2002; 22: 1495-1503Crossref PubMed Scopus (192) Google Scholar, 6Bhatia-Gaur R Donjacour AA Sciavolino PJ Kim M Desai N Young P Norton CR Gridley T Cardiff RD Cunha GR Abate-Shen C Shen MM Roles for Nkx3.1 in prostate development and cancer.Genes Dev. 1999; 13: 966-977Crossref PubMed Scopus (517) Google Scholar An interesting aspect of Nkx3.1 regulation of prostatic proliferation involves the phenomenon of haploinsufficiency. A benign cell has to overcome many obstacles in situ to develop into a fully malignant clone, and the chances of accumulating multiple genetic lesions concurrently in a normal cell are extremely low.20Quon KC Berns A Haplo-insufficiency? Let me count the ways.Genes Dev. 2001; 15: 2917-2921Crossref PubMed Scopus (84) Google Scholar Haploinsufficiency has been proposed as a mechanism by which the efficiency of tumorigenesis can be increased. Loss of a single allele of an haploinsufficient tumor suppressor is sufficient to confer some growth advantage on the mutated cell, thereby expanding the target population in which subsequent mutations can occur. Both p27 and Nkx3.1 have been shown to demonstrate haploinsufficiency. The mechanistic basis for haploinsufficiency in Nkx3.1 mutant mice has begun to be explored. Loss of a single Nkx3.1 allele was found to extend the proliferative phase of luminal epithelial cells of the prostate.7Magee JA Abdulkadir SA Milbrandt J Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation.Cancer Cell. 2003; 3: 273-283Abstract Full Text Full Text PDF PubMed Scopus (117) Google Scholar This is associated with the loss of a subset of exquisitely dosage-sensitive Nkx3.1 target genes. Loss of the second Nkx3.1 allele is associated with dysregulation of another subset of target genes. The results presented here indicate that both p27 and Nkx3.1 regulate prostate epithelial proliferation and development of preneoplastic lesions through both haploinsufficient and nonhaploinsufficient pathways. Partial loss of p27 and Nkx3.1 (ie, compound heterozygosity) did not lead to a significant additive effect on proliferation or development of dysplasia. By contrast, complete loss of both genes resulted in a synergistic increase in proliferation, which is reflected in the increased efficiency with which PIN-like lesions develop. A notable feature of our studies is the finding that complete loss of p27 expression has an effect on the rate of prostatic epithelial cell apoptosis. The apoptotic rate was increased in p27−/− prostates, and this may explain why the prostatic lesions in these animals are limited. Although p27 is primarily involved in regulating the cell cycle, an increase in apoptosis has previously been observed in some tissues of the p27-deficient mouse, for example the retina.21Dyer MA Cepko CL p27Kip1 and p57Kip2 regulate proliferation in distinct retinal progenitor cell populations.J Neurosci. 2001; 21: 4259-4271Crossref PubMed Google Scholar Conversely, in Rb-deficient cells, p27 appears to function as a proapoptotic tumor suppressor.22Carneiro C Jiao MS Hu M Shaffer D Park M Pandolfi PP Cordon-Cardo C Koff A p27 deficiency desensitizes Rb−/− cells to signals that trigger apoptosis during pituitary tumor development.Oncogene. 2003; 22: 361-369Crossref PubMed Scopus (21) Google Scholar Interestingly, our results imply that loss of Nkx3.1 suppresses apoptosis in p27-deficient prostates, because the apoptotic rate in p27−/−Nkx3.1−/− prostates was lower that that in the prostates of p27−/− animals. The precise mechanisms for this phenomenon are presently unclear. Nevertheless, these results suggest that foci of dysplastic cells in PIN lesions that lose both p27 and Nk3.1 protein expression may have an advantage over neighboring cells in both increased proliferation and decreased apoptosis. Our observations indicating that lesions in p27/Nkx3.1 compound mutant mice do not rapidly progress to invasive prostate cancer is consistent with reported observations from several genetically engineered mice not based on SV40 T antigen.14Park JH Walls JE Galvez JJ Kim M Abate-Shen C Shen MM Cardiff RD Prostatic intraepithelial neoplasia in genetically engineered mice.Am J Pathol. 2002; 161: 727-735Abstract Full Text Full Text PDF PubMed Scopus (138) Google Scholar, 23Powell WC Cardiff RD Cohen MB Miller GJ Roy-Burman P Mouse strains for prostate tumorigenesis based on genes altered in human prostate cancer.Curr Drug Targets. 2003; 4: 263-279Crossref PubMed Scopus (24) Google Scholar This has been attributed to the low-proliferative rate of the mouse prostate and the need to disrupt multiple tumorigenic pathways for progression to advanced invasive cancer to occur. Nevertheless, although our studies focus on the roles of Nkx3.1 and p27 in the early stages of prostate tumorigenesis, they do not rule out additional effects of these genes in established tumors. This possibility needs to be entertained because loss of p27 and Nkx3.1 have each been shown to correlate with patient prognosis in human tumors3Bowen C Bubendorf L Voeller HJ Slack R Willi N Sauter G Gasser TC Koivisto P Lack EE Kononen J Kallioniemi OP Gelmann EP Loss of NKX3.1 expression in human prostate cancers correlates with tumor progression.Cancer Res. 2000; 60: 6111-6115PubMed Google Scholar, 24Lloyd RV Erickson LA Jin L Kulig E Qian X Cheville JC Scheithauer BW p27kip1: a multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers.Am J Pathol. 1999; 154: 313-323Abstract Full Text Full Text PDF PubMed Scopus (542) Google Scholar implying that tumors that developed through selection for loss of expression of these proteins are more aggressive. Finally, our studies indicate that p27 and Nkx3.1 play distinct roles in prostate tumor initiation, and that these molecules function by affecting both haploinsufficient and nonhaploinsufficient pathways." @default.
• W1995348626 created "2016-06-24" @default.
• W1995348626 creator A5006903154 @default.
• W1995348626 creator A5017745483 @default.
• W1995348626 creator A5033599611 @default.
• W1995348626 creator A5051171177 @default.
• W1995348626 creator A5066860794 @default.
• W1995348626 creator A5076132197 @default.
• W1995348626 date "2004-05-01" @default.
• W1995348626 modified "2023-09-27" @default.
• W1995348626 title "Interaction of Nkx3.1 and p27kip1 in Prostate Tumor Initiation" @default.
• W1995348626 cites W1495102760 @default.
• W1995348626 cites W1502422706 @default.
• W1995348626 cites W1533487943 @default.
• W1995348626 cites W1538028541 @default.
• W1995348626 cites W1563832763 @default.
• W1995348626 cites W1781630742 @default.
• W1995348626 cites W1969526312 @default.
• W1995348626 cites W1973596168 @default.
• W1995348626 cites W2023862781 @default.
• W1995348626 cites W2029014149 @default.
• W1995348626 cites W2053502484 @default.
• W1995348626 cites W2054740944 @default.
• W1995348626 cites W2061025341 @default.
• W1995348626 cites W2064117760 @default.
• W1995348626 cites W2109193598 @default.
• W1995348626 cites W2111396792 @default.
• W1995348626 cites W2112336517 @default.
• W1995348626 cites W2116711648 @default.
• W1995348626 cites W2118434576 @default.
• W1995348626 cites W2124662269 @default.
• W1995348626 cites W2127757047 @default.
• W1995348626 cites W2138037047 @default.
• W1995348626 cites W2156141690 @default.
• W1995348626 cites W2320432259 @default.
• W1995348626 doi "https://doi.org/10.1016/s0002-9440(10)63719-4" @default.
• W1995348626 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1615644" @default.
• W1995348626 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15111307" @default.
• W1995348626 hasPublicationYear "2004" @default.
• W1995348626 type Work @default.
• W1995348626 sameAs 1995348626 @default.
• W1995348626 citedByCount "35" @default.
• W1995348626 countsByYear W19953486262012 @default.
• W1995348626 countsByYear W19953486262013 @default.
• W1995348626 countsByYear W19953486262014 @default.
• W1995348626 countsByYear W19953486262015 @default.
• W1995348626 countsByYear W19953486262018 @default.
• W1995348626 crossrefType "journal-article" @default.
• W1995348626 hasAuthorship W1995348626A5006903154 @default.
• W1995348626 hasAuthorship W1995348626A5017745483 @default.
• W1995348626 hasAuthorship W1995348626A5033599611 @default.
• W1995348626 hasAuthorship W1995348626A5051171177 @default.
• W1995348626 hasAuthorship W1995348626A5066860794 @default.
• W1995348626 hasAuthorship W1995348626A5076132197 @default.
• W1995348626 hasBestOaLocation W19953486261 @default.
• W1995348626 hasConcept C121608353 @default.
• W1995348626 hasConcept C126322002 @default.
• W1995348626 hasConcept C142724271 @default.
• W1995348626 hasConcept C2776235491 @default.
• W1995348626 hasConcept C71924100 @default.
• W1995348626 hasConcept C86803240 @default.
• W1995348626 hasConceptScore W1995348626C121608353 @default.
• W1995348626 hasConceptScore W1995348626C126322002 @default.
• W1995348626 hasConceptScore W1995348626C142724271 @default.
• W1995348626 hasConceptScore W1995348626C2776235491 @default.
• W1995348626 hasConceptScore W1995348626C71924100 @default.
• W1995348626 hasConceptScore W1995348626C86803240 @default.
• W1995348626 hasIssue "5" @default.
• W1995348626 hasLocation W19953486261 @default.
• W1995348626 hasLocation W19953486262 @default.
• W1995348626 hasLocation W19953486263 @default.
• W1995348626 hasLocation W19953486264 @default.
• W1995348626 hasLocation W19953486265 @default.
• W1995348626 hasOpenAccess W1995348626 @default.
• W1995348626 hasPrimaryLocation W19953486261 @default.
• W1995348626 hasRelatedWork W1966531936 @default.
• W1995348626 hasRelatedWork W1993346425 @default.
• W1995348626 hasRelatedWork W2023033817 @default.
• W1995348626 hasRelatedWork W2030774815 @default.
• W1995348626 hasRelatedWork W2062676201 @default.
• W1995348626 hasRelatedWork W2357527027 @default.
• W1995348626 hasRelatedWork W2410629643 @default.
• W1995348626 hasRelatedWork W2748952813 @default.
• W1995348626 hasRelatedWork W2899084033 @default.
• W1995348626 hasRelatedWork W3031052312 @default.
• W1995348626 hasVolume "164" @default.
• W1995348626 isParatext "false" @default.
• W1995348626 isRetracted "false" @default.
• W1995348626 magId "1995348626" @default.
• W1995348626 workType "article" @default.