Matches in SemOpenAlex for { <https://semopenalex.org/work/W4280601423> ?p ?o ?g. }
- W4280601423 endingPage "590" @default.
- W4280601423 startingPage "577" @default.
- W4280601423 abstract "<p>Aim: The study aims to understand the role of tumor suppressor genes in colorectal cancer initiation and progression. <p> Background: Sporadic colorectal cancer (CRC) develops through distinct molecular events. Loss of the 18q chromosome is a conspicuous event in the progression of adenoma to carcinoma. There is limited information regarding the molecular effectors of this event. Earlier, we had reported ATP8B1 as a novel gene associated with CRC. ATP8B1 belongs to the family of P-type ATPases (P4 ATPase) that primarily function to facilitate the translocation of phospholipids. <p> Objective: In this study, we attempt to implicate the ATP8B1 gene located on chromosome 18q as a tumor suppressor gene. <p> Methods: Cells culture, Patient data analysis, Generation of stable ATP8B1 overexpressing SW480 cell line, Preparation of viral particles, Cell Transduction, Generation of stable ATP8B1 knockdown HT29 cell line with CRISPR/Cas9, Generation of stable ATP8B1 knockdown HT29 cell line with shRNA, Quantification of ATP8B1 gene expression, Real-time cell proliferation and migration assays, Cell proliferation assay, Cell migration assay, Protein isolation and western blotting, Endpoint cell viability assay, Uptake and efflux of sphingolipid, Statistical and computational analyses. <p> Results: We studied indigenous patient data and confirmed the reduced expression of ATP8B1 in tumor samples. CRC cell lines were engineered with reduced and enhanced levels of ATP8B1, which provided a tool to study its role in cancer progression. Forced reduction of ATP8B1 expression either by CRISPR/Cas9 or shRNA was associated with increased growth and proliferation of CRC cell line - HT29. In contrast, overexpression of ATP8B1 resulted in reduced growth and proliferation of SW480 cell lines. We generated a network of genes that are downstream of ATP8B1. Further, we provide the predicted effect of modulation of ATP8B1 levels on this network and the possible effect on fatty acid metabolism-related genes. <p> Conclusion: Tumor suppressor gene (ATP8B1) located on chromosome 18q could be responsible in the progression of colorectal cancer. Knocking down of this gene causes an increased rate of cell proliferation and reduced cell death, suggesting its role as a tumor suppressor. Increasing the expression of this gene in colorectal cancer cells slowed down their growth and increased cell death. These evidences suggest the role of ATP8B1 as a tumor suppressor gene.</p>" @default.
- W4280601423 created "2022-05-22" @default.
- W4280601423 creator A5027034093 @default.
- W4280601423 creator A5035333297 @default.
- W4280601423 creator A5038421285 @default.
- W4280601423 creator A5055074838 @default.
- W4280601423 creator A5071741990 @default.
- W4280601423 creator A5077849310 @default.
- W4280601423 creator A5080592276 @default.
- W4280601423 creator A5083832667 @default.
- W4280601423 date "2022-08-01" @default.
- W4280601423 modified "2023-10-17" @default.
- W4280601423 title "Modulation of ATP8B1 Gene Expression in Colorectal Cancer Cells Suggest its Role as a Tumor Suppressor" @default.
- W4280601423 cites W1486227004 @default.
- W4280601423 cites W1492802549 @default.
- W4280601423 cites W1869365701 @default.
- W4280601423 cites W1966630910 @default.
- W4280601423 cites W1967222064 @default.
- W4280601423 cites W1967700176 @default.
- W4280601423 cites W1968749916 @default.
- W4280601423 cites W1970901908 @default.
- W4280601423 cites W2000047252 @default.
- W4280601423 cites W2005635081 @default.
- W4280601423 cites W2012034410 @default.
- W4280601423 cites W2018063452 @default.
- W4280601423 cites W2020935194 @default.
- W4280601423 cites W2022351047 @default.
- W4280601423 cites W2026469080 @default.
- W4280601423 cites W2032930680 @default.
- W4280601423 cites W2037451457 @default.
- W4280601423 cites W2043829492 @default.
- W4280601423 cites W2045341674 @default.
- W4280601423 cites W2048351097 @default.
- W4280601423 cites W2069369799 @default.
- W4280601423 cites W2072169192 @default.
- W4280601423 cites W2078824719 @default.
- W4280601423 cites W2099001714 @default.
- W4280601423 cites W2109374824 @default.
- W4280601423 cites W2120194191 @default.
- W4280601423 cites W2131040858 @default.
- W4280601423 cites W2152311269 @default.
- W4280601423 cites W2154312575 @default.
- W4280601423 cites W2156236021 @default.
- W4280601423 cites W2340761255 @default.
- W4280601423 cites W2406417533 @default.
- W4280601423 cites W2579357550 @default.
- W4280601423 cites W2749716015 @default.
- W4280601423 cites W2771952185 @default.
- W4280601423 cites W2904365419 @default.
- W4280601423 cites W2910709941 @default.
- W4280601423 cites W3018582544 @default.
- W4280601423 cites W3024801676 @default.
- W4280601423 cites W3090781865 @default.
- W4280601423 doi "https://doi.org/10.2174/1568009622666220517092340" @default.
- W4280601423 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35585825" @default.
- W4280601423 hasPublicationYear "2022" @default.
- W4280601423 type Work @default.
- W4280601423 citedByCount "3" @default.
- W4280601423 countsByYear W42806014232022 @default.
- W4280601423 countsByYear W42806014232023 @default.
- W4280601423 crossrefType "journal-article" @default.
- W4280601423 hasAuthorship W4280601423A5027034093 @default.
- W4280601423 hasAuthorship W4280601423A5035333297 @default.
- W4280601423 hasAuthorship W4280601423A5038421285 @default.
- W4280601423 hasAuthorship W4280601423A5055074838 @default.
- W4280601423 hasAuthorship W4280601423A5071741990 @default.
- W4280601423 hasAuthorship W4280601423A5077849310 @default.
- W4280601423 hasAuthorship W4280601423A5080592276 @default.
- W4280601423 hasAuthorship W4280601423A5083832667 @default.
- W4280601423 hasConcept C104317684 @default.
- W4280601423 hasConcept C121608353 @default.
- W4280601423 hasConcept C173396325 @default.
- W4280601423 hasConcept C29537977 @default.
- W4280601423 hasConcept C502942594 @default.
- W4280601423 hasConcept C54355233 @default.
- W4280601423 hasConcept C555283112 @default.
- W4280601423 hasConcept C62112901 @default.
- W4280601423 hasConcept C81885089 @default.
- W4280601423 hasConcept C86803240 @default.
- W4280601423 hasConcept C95444343 @default.
- W4280601423 hasConcept C98108389 @default.
- W4280601423 hasConceptScore W4280601423C104317684 @default.
- W4280601423 hasConceptScore W4280601423C121608353 @default.
- W4280601423 hasConceptScore W4280601423C173396325 @default.
- W4280601423 hasConceptScore W4280601423C29537977 @default.
- W4280601423 hasConceptScore W4280601423C502942594 @default.
- W4280601423 hasConceptScore W4280601423C54355233 @default.
- W4280601423 hasConceptScore W4280601423C555283112 @default.
- W4280601423 hasConceptScore W4280601423C62112901 @default.
- W4280601423 hasConceptScore W4280601423C81885089 @default.
- W4280601423 hasConceptScore W4280601423C86803240 @default.
- W4280601423 hasConceptScore W4280601423C95444343 @default.
- W4280601423 hasConceptScore W4280601423C98108389 @default.
- W4280601423 hasFunder F4320327902 @default.
- W4280601423 hasIssue "7" @default.
- W4280601423 hasLocation W42806014231 @default.
- W4280601423 hasLocation W42806014232 @default.
- W4280601423 hasOpenAccess W4280601423 @default.