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        <datestamp>2026-09-23T09:00:04Z</datestamp>
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          <dc:title>Identification of anoikis-related and cell matrix adhesion genes in the progression of colon adenocarcinoma using bioinformatics analysis</dc:title>
          <dc:creator>Ting Zheng (608653)</dc:creator>
          <dc:creator>Xingxing Li (321490)</dc:creator>
          <dc:creator>Li Zhou (54356)</dc:creator>
          <dc:creator>Jianjiang Jin (22813439)</dc:creator>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Mathematical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Anoikis</dc:subject>
          <dc:subject>cell-matrix adhesion</dc:subject>
          <dc:subject>colon adenocarcinoma</dc:subject>
          <dc:subject>risk model</dc:subject>
          <dc:subject>prognosis</dc:subject>
          <dc:description>&lt;p&gt;To develop an innovative prognostic model for colon adenocarcinoma (COAD), we integated anoikis- and cell matrix adhesion (CMA related mechanisms using TCGA and GEO datasets. Six genes (BST2, NAT1, OFCC1, HOTAIR, TRIP6, ADAMTS13) were identified, risk model stratified patients into high- and low risk groups with distinct survival (p=0.025), validated in GSE17536. A nomogram showed good predictive accuracy. Functional enrichment highlighted tumor-, anoikis-, and CMA-related pathways, immune infiltration correlated with prognostic signature and risk score. High-risk patients were more sensitive to afatinib, osimertinib, and navitoclax; low-risk patients to paclitaxel, docetaxel, and gemcitabine. These genes may serve as prognostic biomarkers and guide tailored COAD therapy.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-23T09:00:04Z</dc:date>
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