Scholarlink

<p>Metastatic colorectal cancer (mCRC) differs clinically based on <i>RAS</i> and <i>BRAF</i> mutations or DNA methylation. However, in mCRC, the prognostic value and biological characteristics of genome-wide DNA methylation status (GWMS) in each <i>RAS/BRAF</i> genotype is unknown. To clarify this, primary tumor samples from patients with informed consent in the phase III TRICOLORE study were collected, and <i>RAS</i> and <i>BRAF</i> mutations, immunohistochemical staining of mismatch repair-related proteins, comprehensive gene expression, and genome-wide DNA methylation were analyzed. The tumor samples were classified into high-methylated colorectal cancer (HMCC) and low-methylated colorectal cancer (LMCC). Gene set enrichment analysis (GSEA) was conducted using microarray data. A total of 226 patients were included and classified into the <i>RAS</i>/<i>BRAF</i> wild-type (wt) (n = 125), <i>RAS</i> mutant (mt) (n = 87), and <i>BRAF</i> mt (n = 14), of whom 22 (17.6%), 30 (34.5%), and 14 (100%) had HMCC. HMCC exhibited significantly worse overall survival (OS) than that of LMCC in the <i>RAS</i>/<i>BRAF</i> wt group but not in the <i>RAS</i> mt group. In GSEA, <i>RAS</i>/<i>BRAF</i> wt HMCC was associated with microsatellite instability and <i>BRAF</i> V600E mutation. The poor prognosis of <i>RAS/BRAF</i> wt HMCC may be attributed to gene expression patterns associated with microsatellite instability and <i>BRAF</i> V600E mutation.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

RAS/BRAF wild-type metastatic high-methylated colorectal cancer has gene expression patterns related to MSI-H and BRAF V600E mutant: a translational research

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月8日

查看全文
  • Shonosuke Wakayama,
  • Shin Takahashi,
  • Kota Ouchi,
  • Yasuhiro Sakamoto,
  • Tadamichi Denda,
  • Atsuo Takashima,
  • Yoshito Komatsu,
  • Masato Nakamura,
  • Hisatsugu Ohori,
  • Tatsuro Yamaguchi,
  • Yoshimitsu Kobayashi,
  • Hideo Baba,
  • Masanori Kotake,
  • Kenji Amagai,
  • Hitoshi Kondo,
  • Ken Shimada,
  • Yasuhide Yamada,
  • Atsushi Sato,
  • Satoshi Yuki,
  • Akira Okita,
  • Keigo Komine,
  • Mika Watanabe,
  • Satoshi Morita,
  • Chikashi Ishioka

摘要

Metastatic colorectal cancer (mCRC) differs clinically based on RAS and BRAF mutations or DNA methylation. However, in mCRC, the prognostic value and biological characteristics of genome-wide DNA methylation status (GWMS) in each RAS/BRAF genotype is unknown. To clarify this, primary tumor samples from patients with informed consent in the phase III TRICOLORE study were collected, and RAS and BRAF mutations, immunohistochemical staining of mismatch repair-related proteins, comprehensive gene expression, and genome-wide DNA methylation were analyzed. The tumor samples were classified into high-methylated colorectal cancer (HMCC) and low-methylated colorectal cancer (LMCC). Gene set enrichment analysis (GSEA) was conducted using microarray data. A total of 226 patients were included and classified into the RAS/BRAF wild-type (wt) (n = 125), RAS mutant (mt) (n = 87), and BRAF mt (n = 14), of whom 22 (17.6%), 30 (34.5%), and 14 (100%) had HMCC. HMCC exhibited significantly worse overall survival (OS) than that of LMCC in the RAS/BRAF wt group but not in the RAS mt group. In GSEA, RAS/BRAF wt HMCC was associated with microsatellite instability and BRAF V600E mutation. The poor prognosis of RAS/BRAF wt HMCC may be attributed to gene expression patterns associated with microsatellite instability and BRAF V600E mutation.