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m6 RNA甲基化调节因子KIAA1429与肺癌中自噬介导的耐药性相关。

The m6 RNA methylation regulator KIAA1429 is associated with autophagy-mediated drug resistance in lung cancer.

作者信息

Ma Bo, Xiu Lei, Ding Lili

机构信息

Department of General Thoracic Surgery General Hospital of Ningxia Medical University Yinchuan China.

Department of Thoracic and Cardiac Surgery General Hospital of Ningxia Medical University Yinchuan China.

出版信息

FASEB Bioadv. 2024 Mar 15;6(4):105-117. doi: 10.1096/fba.2023-00083. eCollection 2024 Apr.

Abstract

N6-methyladenosine (m6A) modification plays a crucial role in cancer progression. However, the role of m6A modification-mediated autophagy underlying non-small cell lung cancer (NSCLC) gefitinib resistance remains unknown. Here, we discovered that m6A methyltransferase KIAA1429 was highly expressed in NSCLC gefitinib-resistant cells (PC9-GR) as well as tissues, and KIAA1429 high expression was associated with poor survival. In addition, silent KIAA1429 repressed gefitinib resistance in NSCLC and reduced tumor growth in vivo. Mechanistically, KIAA1429 stabilized WTAP, a significant player in autophagy, by binding to the 3' untranslated regions (3'-UTR) of WTAP. In a word, our findings indicated that KIAA1429 could elevate NSCLC gefitinib resistance, which may provide a promising targeted therapy for NSCLC patients.

摘要

N6-甲基腺苷(m6A)修饰在癌症进展中起着关键作用。然而,m6A修饰介导的自噬在非小细胞肺癌(NSCLC)吉非替尼耐药中的作用仍不清楚。在此,我们发现m6A甲基转移酶KIAA1429在NSCLC吉非替尼耐药细胞(PC9-GR)以及组织中高表达,且KIAA1429高表达与较差的生存率相关。此外,沉默KIAA1429可抑制NSCLC中的吉非替尼耐药并减少体内肿瘤生长。机制上,KIAA1429通过与WTAP的3'非翻译区(3'-UTR)结合来稳定WTAP,WTAP是自噬中的一个重要因子。总之,我们的研究结果表明KIAA1429可提高NSCLC对吉非替尼的耐药性,这可能为NSCLC患者提供一种有前景的靶向治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d95c/10995705/a7ce8bf775e9/FBA2-6-105-g001.jpg

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