論文

国際誌
2021年4月

Integrin-linked kinase pathway in heterogeneous pulmonary sarcomatoid carcinoma.

Oncology letters
  • Shigeki Shimizu
  • ,
  • Kazuko Sakai
  • ,
  • Takaaki Chikugo
  • ,
  • Takao Satou
  • ,
  • Naoki Shiraishi
  • ,
  • Tetsuya Mitsudomi
  • ,
  • Kazuto Nishio

21
4
開始ページ
320
終了ページ
320
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3892/ol.2021.12582

Pulmonary sarcomatoid carcinoma (PSC) is classified as poorly differentiated, and non-small cell lung carcinomas that contained a component of sarcoma or sarcoma-like differentiation are rare. The underlying carcinogenetic mechanism governing PSC remains unclear. The current study investigated the underlying carcinogenetic mechanism of PSC based on the hypothesis that it involves the epithelial-mesenchymal transition (EMT) process. Mutation analysis of PSCs, including carcinosarcoma, pleomorphic carcinoma and epithelial carcinoma specimens, was performed using targeted deep sequencing, whole transcriptome analysis and digital spatial profiling (DSP). PSCs exhibit a distinct mutation profile, with TP53, SYNE1 and APC mutations. Therefore, clustering of the gene expression profiles allowed the PSCs to be distinguished from the epithelial carcinomas. Increased gene expression of fibronectin in PSC was an important contributor to differential profiles. Pathway analysis revealed enhanced activity of the integrin-linked kinase (ILK) signaling pathway in the PSCs. DSP analysis using 56 antibodies of marker proteins confirmed significantly higher expression of fibronectin in PSCs. Intratumor heterogeneity of fibronectin expression was observed in sarcoma components. In conclusion, epithelial-mesenchymal transition process mediated by ILK signaling may be associated with carcinogenetic mechanisms of PSC. Overexpression of fibronectin mediated by ILK signaling appears to serve a role in the EMT involved in the PSC transformation process.

リンク情報
DOI
https://doi.org/10.3892/ol.2021.12582
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/33692852
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933776
ID情報
  • DOI : 10.3892/ol.2021.12582
  • PubMed ID : 33692852
  • PubMed Central 記事ID : PMC7933776

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