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Tobacco carcinogen NNK promotes pancreatic cancer proliferation via LINC00857/β-catenin

  • Cancan Zhou
  • , Ruiqi Cao
  • , Qiqi Wang
  • , Jiantao Mo
  • , Weikun Qian
  • , Zhengyuan Feng
  • , Shengzhan Zhang
  • , Xin Chen
  • , Jie Hao
  • , Qingyong Ma
  • , Zheng Wu
  • , Zheng Wang
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Xi'an Jiaotong University

科研成果: 期刊稿件 › 文章 › 同行评审

1 引用 (Scopus)

摘要

INTRODUCTION Smoking is a key risk factor for pancreatic cancer (PC). Nicotine-derived nitrosamine ketone (NNK), a major tobacco smoke constituent, has been shown to promote cancer growth, but its specific role in PC progression remains unclear. While long non-coding RNA LINC00857 (lnc RNA) is implicated in cancer progression, its regulation by NNK is unknown. This study aims to investigate whether NNK can drive PC growth and elucidate the underlying mechanisms. METHODS Employing an experimental methodology, this investigation treated human pancreatic cancer cell lines (CFPAC-1 and Panc-1) with NNK and utilized various assays (CCK-8, colony formation, and EdU cell proliferation) to assess the effects on cell proliferation. The interplay between LINC00857 expression profiles, PC, and smoking was systematically investigated through cross-database bioinformatic interrogation encompassing public resources and institutional biobank data. Experiments were performed to knock down LINC00857 in PC cells using siRNA technology. We used Western blotting and quantitative real-time PCR (qRT-PCR) to assess β-catenin expression and elucidate the mechanism by which the tobacco carcinogen NNK promotes PC formation. RESULTS Some evidence that NNK enhanced the proliferative capacity of PC cells was found. Bioinformatic analysis of public databases, combined with data from our center's database, revealed that LINC00857 was up-regulated in PC and correlated with smoking. Moreover, we discovered that knockdown of LINC00857 inhibited PC cell proliferation, with β-catenin identified as a potential downstream molecule. Importantly, after LINC00857 knockdown, we observed suppression of NNK-induced β-catenin upregulation at both protein and transcriptional levels. CONCLUSIONS NNK potentially induces PC progression through the LINC00857/βcatenin axis. These findings provide new perspectives on the mechanisms of PC progression and highlight the clinical relevance of smoking cessation for preventing PC.

源语言英语
期刊论文编号50
期刊Tobacco Induced Diseases
卷23
DOI
出版状态已出版 - 4月 2025

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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