1. Academic Validation
  2. METTL3 promotes chemoresistance in small cell lung cancer by inducing mitophagy

METTL3 promotes chemoresistance in small cell lung cancer by inducing mitophagy

  • J Exp Clin Cancer Res. 2023 Mar 17;42(1):65. doi: 10.1186/s13046-023-02638-9.
Yueqin Sun # 1 Weitao Shen # 1 Shulu Hu # 1 Qiong Lyu # 1 Qiongyao Wang 1 Ting Wei 2 Weiliang Zhu 3 Jian Zhang 4
Affiliations

Affiliations

  • 1 Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
  • 2 Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China. weitingyouyou@qq.com.
  • 3 Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China. duarion@126.com.
  • 4 Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China. zhangjian@i.smu.edu.cn.
  • # Contributed equally.
Abstract

Background: Small cell lung Cancer (SCLC) is the most aggressive subtype of lung Cancer. Although most patients are initially sensitive to first-line combination chemotherapy with cisplatin and etoposide, chemotherapy drug resistance easily develops and quickly leads to tumour progression. Therefore, understanding the mechanisms of chemotherapy drug resistance and how to reverse it is key to improving the prognosis of patients with SCLC. Moreover, N6-methyladenosine (m6A) is the most abundant mRNA modification and is catalysed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit.

Methods: The effects of METTL3 on chemoresistance in SCLC cells were determined using qRT-PCR, Western blotting, immunohistochemistry, cell counting kit (CCK-8) assays, flow cytometry, and tumorigenicity experiments. Methylated RNA immunoprecipitation Sequencing (MeRIP-seq), MeRIP qPCR, immunofluorescence, and drug inhibitor experiments were performed to confirm the molecular mechanism of Decapping Protein 2 (DCP2), which is involved in the chemoresistance of SCLC.

Results: In the present study, we found that METTL3 is a marker for poor SCLC prognosis, and it is highly expressed in chemoresistant SCLC cells. METTL3 promotes SCLC chemoresistance by positively regulating Mitophagy. METTL3 induces m6A methylation of DCP2 and causes the degradation of DCP2, which promotes mitochondrial Autophagy through the Pink1-Parkin pathway, leading to chemotherapy resistance. We also found that STM2457, a novel METTL3 Inhibitor, can reverse SCLC chemoresistance.

Conclusions: The m6A methyltransferase METTL3 regulates Pink1-Parkin pathway-mediated Mitophagy and mitochondrial damage in SCLC cells by targeting DCP2, thereby promoting chemotherapy resistance in patients with SCLC.

Keywords

Chemoresistance; Mitophagy; N6-methyladenosine; Small cell lung cancer.

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