Targeting fatty acid synthase suppresses tumor development in NF2/CDKN2A-deficient malignant pleural mesothelioma

Sivasundaram Karnan; Akinobu Ota; Muhammad Nazmul Hasan; Hideki Murakami; Md Lutfur Rahman; Md Wahiduzzaman; Md Towhid Ahmed Shihan; Nushrat Jahan; Lam Quang Vu; Ichiro Hanamura; Akihito Inoko; Miho Riku; Hideaki Ito; Yoshifumi Kaneko; Yinzhi Lin; Toshinori Hyodo; Hiroyuki Konishi; Shinobu Tsuzuki; Yoshitaka Hosokawa

doi:10.1038/s41419-026-08481-y

Cancer BiologyCell Death and DiseaseFeb 28, 2026

Peer-reviewed journal article

Targeting fatty acid synthase suppresses tumor development in NF2/CDKN2A-deficient malignant pleural mesothelioma

Sivasundaram Karnan iD, Akinobu Ota iD, Muhammad Nazmul Hasan iD, Hideki Murakami iD, Md Lutfur Rahman iD, Md Wahiduzzaman iD, Md Towhid Ahmed Shihan, Nushrat Jahan, Lam Quang Vu, Ichiro Hanamura iD, Akihito Inoko iD, Miho Riku iD, Hideaki Ito, Yoshifumi Kaneko, Yinzhi Lin iD, Toshinori Hyodo iD, Hiroyuki Konishi iD, Shinobu Tsuzuki iD, Yoshitaka Hosokawa iD

Abstract

Malignant pleural mesothelioma (MPM) is an uncommon yet deadly cancer linked to asbestos exposure. The lack of effective early diagnosis and treatment leads to reduced life expectancy among patients with MPM. This study is aimed to identify a novel molecular target inhibitor to develop more effective therapeutics for MPM. Our drug screening assay showed that the fatty acid synthase (FASN) inhibitor cerulenin demonstrates strong and selective anti-proliferative properties against NF2/CDKN2A(p16)-deficient MPM cells, surpassing the effects of cisplatin or pemetrexed. FASN protein is frequently detected in NF2/p16-deficient MPM tumor-derived tissues (15/15, 100%), but rarely in NF2/p16-intact MPM tumors (8/25, 32%). Notably, cerulenin administration successfully reduced the growth of NF2/p16-deficient MPM tumors in xenografted mice. Cerulenin inhibits mitochondrial fission by targeting dynamin-related protein 1 (DRP1) in NF2/p16-deficient cells. Moreover, the disruption of the FASN gene leads to increased ubiquitination of DRP1. These findings suggest that FASN might play a role in the tumorigenesis of MPM cells through the regulation of mitochondrial dynamics. This research offers a novel perspective on the potential development of precision medicine for MPM.

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