Matches in SemOpenAlex for { <https://semopenalex.org/work/W2892280080> ?p ?o ?g. }
- W2892280080 abstract "The ectopic HLA-G expression in malignancies has been extensively explored and clinical significance of the molecule was widely acknowledged. Besides previously well-documented seven isoforms (HLA-G1~-G7), other novel isoforms of HLA-G have been reported but their clinical relavenace remians evaluated. In this study, lesion HLA-G expression in 379 case-matched serial section primary colorectal cancers (CRC) were evaluated with mAb 4H84 (recognizing an epitope in HLA-G α1 domain), and mAb 5A6G7 (recognizing an epitope encoded by intron 5), respectively. Data showed that HLA-G positive staining with mAbs 4H84 and 5A6G7 was 70.7% and 60.4%, respectively. When percentage of HLA-G expression detected with mAb 4H84 subtracted that with mAb 5A6G7, the difference (∆HLA-G) with negative (∆HLA-Gneg), comparable (∆HLA-Gcom) and positive (∆HLA-Gpos) were observed in 64 (16.9%), 159 (42.0%) and 156 (41.2%) cases, respectively. Noteworthy, unexpected immunostaining was observed in 44 (11.6%) lesions that no staining was detected with mAb 4H84 but positive with mAb 5A6G7 (4H84neg5A6G7pos). This staining pattern was unpredictable because all seven known HLA-G isoforms containing the α 1 domain could be recognized by the mAb 4H84. Moreover, patients with ∆HLA-Gneg had obviously better survival than those with ∆HLA-Gcom and ∆HLA-Gpos (p=0.017), and ∆HLA-G could be an independent prognostic factor for CRC patients (p=0.008). Our findings provides the first report that potential unidentified HLA-G isoforms is of distinct clinical significance in CRC patients." @default.
- W2892280080 created "2018-09-27" @default.
- W2892280080 creator A5000626725 @default.
- W2892280080 creator A5035771855 @default.
- W2892280080 creator A5062857757 @default.
- W2892280080 creator A5075681541 @default.
- W2892280080 creator A5082457297 @default.
- W2892280080 creator A5090875147 @default.
- W2892280080 date "2018-09-04" @default.
- W2892280080 modified "2023-10-18" @default.
- W2892280080 title "Clinical Significance of Potential Unidentified HLA-G Isoforms Without α1 Domain but Containing Intron 4 in Colorectal Cancer Patients" @default.
- W2892280080 cites W144482947 @default.
- W2892280080 cites W1561153455 @default.
- W2892280080 cites W1571885793 @default.
- W2892280080 cites W1978187098 @default.
- W2892280080 cites W1985043455 @default.
- W2892280080 cites W1985213644 @default.
- W2892280080 cites W1985965155 @default.
- W2892280080 cites W1986672594 @default.
- W2892280080 cites W1999752919 @default.
- W2892280080 cites W2003768623 @default.
- W2892280080 cites W2011674123 @default.
- W2892280080 cites W2012671068 @default.
- W2892280080 cites W2015650992 @default.
- W2892280080 cites W2023495487 @default.
- W2892280080 cites W2024708677 @default.
- W2892280080 cites W2035155248 @default.
- W2892280080 cites W2043731481 @default.
- W2892280080 cites W2046495164 @default.
- W2892280080 cites W2048332030 @default.
- W2892280080 cites W2049656655 @default.
- W2892280080 cites W2050525926 @default.
- W2892280080 cites W2064086926 @default.
- W2892280080 cites W2067735015 @default.
- W2892280080 cites W2070598430 @default.
- W2892280080 cites W2088513266 @default.
- W2892280080 cites W2093879671 @default.
- W2892280080 cites W2108463809 @default.
- W2892280080 cites W2108819691 @default.
- W2892280080 cites W2142982199 @default.
- W2892280080 cites W2148712229 @default.
- W2892280080 cites W2160048269 @default.
- W2892280080 cites W2166126168 @default.
- W2892280080 cites W2190245867 @default.
- W2892280080 cites W2428513144 @default.
- W2892280080 cites W2462192596 @default.
- W2892280080 cites W2549171424 @default.
- W2892280080 cites W2597872842 @default.
- W2892280080 cites W2750487285 @default.
- W2892280080 cites W2768159192 @default.
- W2892280080 cites W2778954208 @default.
- W2892280080 cites W2790774912 @default.
- W2892280080 cites W2795041265 @default.
- W2892280080 cites W608522650 @default.
- W2892280080 doi "https://doi.org/10.3389/fonc.2018.00361" @default.
- W2892280080 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6131604" @default.
- W2892280080 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30234020" @default.
- W2892280080 hasPublicationYear "2018" @default.
- W2892280080 type Work @default.
- W2892280080 sameAs 2892280080 @default.
- W2892280080 citedByCount "21" @default.
- W2892280080 countsByYear W28922800802019 @default.
- W2892280080 countsByYear W28922800802020 @default.
- W2892280080 countsByYear W28922800802021 @default.
- W2892280080 countsByYear W28922800802022 @default.
- W2892280080 countsByYear W28922800802023 @default.
- W2892280080 crossrefType "journal-article" @default.
- W2892280080 hasAuthorship W2892280080A5000626725 @default.
- W2892280080 hasAuthorship W2892280080A5035771855 @default.
- W2892280080 hasAuthorship W2892280080A5062857757 @default.
- W2892280080 hasAuthorship W2892280080A5075681541 @default.
- W2892280080 hasAuthorship W2892280080A5082457297 @default.
- W2892280080 hasAuthorship W2892280080A5090875147 @default.
- W2892280080 hasBestOaLocation W28922800801 @default.
- W2892280080 hasConcept C104317684 @default.
- W2892280080 hasConcept C121608353 @default.
- W2892280080 hasConcept C126322002 @default.
- W2892280080 hasConcept C142724271 @default.
- W2892280080 hasConcept C147483822 @default.
- W2892280080 hasConcept C153911025 @default.
- W2892280080 hasConcept C159654299 @default.
- W2892280080 hasConcept C188280979 @default.
- W2892280080 hasConcept C195616568 @default.
- W2892280080 hasConcept C203014093 @default.
- W2892280080 hasConcept C204232928 @default.
- W2892280080 hasConcept C2780027760 @default.
- W2892280080 hasConcept C4224716 @default.
- W2892280080 hasConcept C502942594 @default.
- W2892280080 hasConcept C526805850 @default.
- W2892280080 hasConcept C53345823 @default.
- W2892280080 hasConcept C542903549 @default.
- W2892280080 hasConcept C54355233 @default.
- W2892280080 hasConcept C63363279 @default.
- W2892280080 hasConcept C71924100 @default.
- W2892280080 hasConcept C86803240 @default.
- W2892280080 hasConcept C94671646 @default.
- W2892280080 hasConceptScore W2892280080C104317684 @default.
- W2892280080 hasConceptScore W2892280080C121608353 @default.
- W2892280080 hasConceptScore W2892280080C126322002 @default.
- W2892280080 hasConceptScore W2892280080C142724271 @default.