<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(7)</volume><submitter>Huang W</submitter><pubmed_abstract>Chemoresistance remains the primary challenge of clinical treatment of gastric cancer (GC), making the biomarkers of chemoresistance crucial for treatment decision. Our previous study has reported that p21-actived kinase 6 (PAK6) is a prognostic factor for selecting which patients with GC are resistant to 5-fluorouracil/oxaliplatin chemotherapy. However, the mechanistic role of PAK6 in chemosensitivity remains unknown. The present study identified PAK6 as an important modulator of the DNA damage response (DDR) and chemosensitivity in GC. Analysis of specimens from patients revealed significant associations between the expression of PAK6 and poorer stages, deeper invasion, more lymph node metastases, higher recurrence rates, and resistance to oxaliplatin. Cells exhibited chemosensitivity to</pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>658</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9334622</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PAK6 promotes homologous-recombination to enhance chemoresistance to oxaliplatin through ATR/CHK1 signaling in gastric cancer.</pubmed_title><pmcid>PMC9334622</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Yuan Q</pubmed_authors><pubmed_authors>Han Z</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Sun Z</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Feng H</pubmed_authors></additional><is_claimable>false</is_claimable><name>PAK6 promotes homologous-recombination to enhance chemoresistance to oxaliplatin through ATR/CHK1 signaling in gastric cancer.</name><description>Chemoresistance remains the primary challenge of clinical treatment of gastric cancer (GC), making the biomarkers of chemoresistance crucial for treatment decision. Our previous study has reported that p21-actived kinase 6 (PAK6) is a prognostic factor for selecting which patients with GC are resistant to 5-fluorouracil/oxaliplatin chemotherapy. However, the mechanistic role of PAK6 in chemosensitivity remains unknown. The present study identified PAK6 as an important modulator of the DNA damage response (DDR) and chemosensitivity in GC. Analysis of specimens from patients revealed significant associations between the expression of PAK6 and poorer stages, deeper invasion, more lymph node metastases, higher recurrence rates, and resistance to oxaliplatin. Cells exhibited chemosensitivity to</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-18T22:26:37.911Z</modification><creation>2025-04-07T10:13:48.951Z</creation></dates><accession>S-EPMC9334622</accession><cross_references><pubmed>35902562</pubmed><doi>10.1038/s41419-022-05118-8</doi></cross_references></HashMap>