Matches in SemOpenAlex for { <https://semopenalex.org/work/W2004682208> ?p ?o ?g. }
- W2004682208 endingPage "504" @default.
- W2004682208 startingPage "491" @default.
- W2004682208 abstract "In the present study, we evaluated the antitumor effect of two synthetic analogs of vitamin D, namely PRI-2191 [(24R)-1,24-dihydroxyvitamin D3] and PRI-2205 (5,6-trans calcipotriol), in combined human colon HT-29 cancer treatment with 5-fluorouracil (5-FU). Mice bearing HT-29 tumors transplanted subcutaneously or orthotopically were injected with vitamin D analogs and 5-FU in various schedules. A statistically significant inhibition of subcutaneous or orthotopic tumor growth was observed as a result of combined therapy. In HT-29 tumors and in cells from in vitro culture, we observed increased vitamin D receptor (VDR) expression after treatment with either PRI-2205 or 5-FU alone, or in combination. Moreover, PRI-2205 decreased the percentage of cells from intestinal tumors in G2/M and S stages and increased sub-G1. Increased VDR expression was also observed after combined treatment of mice with 5-FU and PRI-2191. Moreover, our docking studies showed that PRI-2205 has stronger affinity for VDR, DBP and CAR/RXR ligand binding domains than PRI-2191. PRI-2191 analog, used with 5-FU, increased the percentage of subcutaneous tumor cells in G0/G1 and decreased the percentage in G2/M, S and sub-G1 populations as compared to 5-FU alone. In in vitro studies, we observed increased expression of p21 and p-ERK1/2 diminution via use of both analogs as compared to use of 5-FU alone. Simultaneously, PRI-2191 antagonizes some pro-apoptotic activities of 5-FU in vitro. However, in spite of these disadvantageous effects in terms of apoptosis, the therapeutic effect expressed as tumor growth retardation by PRI-2191 is significant. Our results suggest that the mechanism of potentiation of 5-FU antitumor action by both analogs is realized via increased p21 expression and decreased p-ERK1/2 level which may lead to diminution of thymidylate synthase expression. Higher binding affinity for VDR, DBP, but also for CARRXR ligand binding domain of PRI-2205 may, in part, explain its very low toxicity with sustained anticancer activity." @default.
- W2004682208 created "2016-06-24" @default.
- W2004682208 creator A5000580616 @default.
- W2004682208 creator A5006439255 @default.
- W2004682208 creator A5022446752 @default.
- W2004682208 creator A5044807382 @default.
- W2004682208 creator A5052033965 @default.
- W2004682208 date "2014-06-11" @default.
- W2004682208 modified "2023-09-26" @default.
- W2004682208 title "Vitamin D analogs combined with 5-fluorouracil in human HT-29 colon cancer treatment" @default.
- W2004682208 cites W1498442525 @default.
- W2004682208 cites W1535821387 @default.
- W2004682208 cites W1874198797 @default.
- W2004682208 cites W1967992011 @default.
- W2004682208 cites W1969688760 @default.
- W2004682208 cites W1972964586 @default.
- W2004682208 cites W1973391025 @default.
- W2004682208 cites W1978006133 @default.
- W2004682208 cites W1982251648 @default.
- W2004682208 cites W1982294311 @default.
- W2004682208 cites W1984328540 @default.
- W2004682208 cites W1985588649 @default.
- W2004682208 cites W1997060393 @default.
- W2004682208 cites W2009423060 @default.
- W2004682208 cites W2012551902 @default.
- W2004682208 cites W2019134138 @default.
- W2004682208 cites W2031168104 @default.
- W2004682208 cites W2034564140 @default.
- W2004682208 cites W2035662091 @default.
- W2004682208 cites W2036430139 @default.
- W2004682208 cites W2036889297 @default.
- W2004682208 cites W2040120466 @default.
- W2004682208 cites W2041739283 @default.
- W2004682208 cites W2053516868 @default.
- W2004682208 cites W2054917615 @default.
- W2004682208 cites W2064325782 @default.
- W2004682208 cites W2065195395 @default.
- W2004682208 cites W2068581230 @default.
- W2004682208 cites W2069395010 @default.
- W2004682208 cites W2073599728 @default.
- W2004682208 cites W2076151897 @default.
- W2004682208 cites W2081894694 @default.
- W2004682208 cites W2084065462 @default.
- W2004682208 cites W2093903659 @default.
- W2004682208 cites W2094281679 @default.
- W2004682208 cites W2095259916 @default.
- W2004682208 cites W2102377211 @default.
- W2004682208 cites W2103269630 @default.
- W2004682208 cites W2110061723 @default.
- W2004682208 cites W2112956266 @default.
- W2004682208 cites W2114764370 @default.
- W2004682208 cites W2125380516 @default.
- W2004682208 cites W2127058741 @default.
- W2004682208 cites W2129152244 @default.
- W2004682208 cites W2132559227 @default.
- W2004682208 cites W2137850244 @default.
- W2004682208 cites W2138153315 @default.
- W2004682208 cites W2140247386 @default.
- W2004682208 cites W2142868265 @default.
- W2004682208 cites W2150118613 @default.
- W2004682208 cites W2150524562 @default.
- W2004682208 cites W2151249459 @default.
- W2004682208 cites W2153523313 @default.
- W2004682208 cites W2166420696 @default.
- W2004682208 cites W2166765429 @default.
- W2004682208 cites W2414954258 @default.
- W2004682208 doi "https://doi.org/10.3892/or.2014.3247" @default.
- W2004682208 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4091879" @default.
- W2004682208 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24919507" @default.
- W2004682208 hasPublicationYear "2014" @default.
- W2004682208 type Work @default.
- W2004682208 sameAs 2004682208 @default.
- W2004682208 citedByCount "40" @default.
- W2004682208 countsByYear W20046822082014 @default.
- W2004682208 countsByYear W20046822082015 @default.
- W2004682208 countsByYear W20046822082016 @default.
- W2004682208 countsByYear W20046822082017 @default.
- W2004682208 countsByYear W20046822082018 @default.
- W2004682208 countsByYear W20046822082019 @default.
- W2004682208 countsByYear W20046822082020 @default.
- W2004682208 countsByYear W20046822082021 @default.
- W2004682208 countsByYear W20046822082022 @default.
- W2004682208 countsByYear W20046822082023 @default.
- W2004682208 crossrefType "journal-article" @default.
- W2004682208 hasAuthorship W2004682208A5000580616 @default.
- W2004682208 hasAuthorship W2004682208A5006439255 @default.
- W2004682208 hasAuthorship W2004682208A5022446752 @default.
- W2004682208 hasAuthorship W2004682208A5044807382 @default.
- W2004682208 hasAuthorship W2004682208A5052033965 @default.
- W2004682208 hasBestOaLocation W20046822081 @default.
- W2004682208 hasConcept C121608353 @default.
- W2004682208 hasConcept C124490489 @default.
- W2004682208 hasConcept C126322002 @default.
- W2004682208 hasConcept C134018914 @default.
- W2004682208 hasConcept C170493617 @default.
- W2004682208 hasConcept C179639408 @default.
- W2004682208 hasConcept C185592680 @default.
- W2004682208 hasConcept C190283241 @default.