Pan‐HER inhibitors overcome lorlatinib resistance caused by NRG1/HER3 activation in ALK‐rearranged lung cancer. Issue 1 (21st September 2022)

• Record Type: Journal Article
• Authors: Taniguchi, Hirokazu; Akagi, Kazumasa; Dotsu, Yosuke; Yamada, Tadaaki; Ono, Sawana; Imamura, Erika; Gyotoku, Hiroshi; Takemoto, Shinnosuke; Yamaguchi, Hiroyuki; Sen, Triparna; Yano, Seiji; Mukae, Hiroshi
• Is Part Of: Cancer science. Volume 114:Issue 1(2023)
• Page Start: 164
• Page End: 173
• Publication Date: 2022-09-21
• Subjects: ALK inhibitor -- drug resistance -- HER3 -- lorlatinib -- non–small‐cell lung cancer; Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.15579
• Languages: English
• ISSNs: 1347-9032

Abstract

Abstract: Lorlatinib, a third‐generation anaplastic lymphoma kinase (ALK)‐tyrosine kinase inhibitor (TKI) with a broad coverage against ALK mutations, has demonstrated dramatic effects in patients with ALK ‐rearranged lung cancer. The mechanisms of acquired resistance to lorlatinib by secondary ALK compound mutations have recently been reported; however, resistance mechanisms other than secondary mutations remain unclear. Here, we investigated the molecular mechanisms of the acquired resistance in ALK ‐rearranged lung cancer cells in vitro. We established two different lorlatinib‐resistant ALK ‐rearranged lung cancer cell lines (H3122LR and A925LLR) via long‐term administration of lorlatinib. These resistant cells did not harbor the secondary ALK mutations and showed cross‐resistance to the other kinds of ALK‐TKIs (crizotinib or alectinib) compared with the parental cells; however, these resistant cells overexpressed the phosphorylated human epidermal growth factor receptor 3 (HER3) protein and the ligand of HER3 (neuregulin 1; NRG1). Pharmacological inhibition of HER3 with pan‐HER inhibitors or genetic knockdown of HER3 with siRNA resensitized H3122LR and A925LLR cells to lorlatinib in vitro, indicating that H3122LR and A925LLR acquired resistance by NRG1/HER3 activation. These findings demonstrated that targeting NRG1/HER3 is a potential novel therapeutic option for lorlatinib‐resistant ALK ‐rearranged lung cancer. Abstract : In the present study, we induced lorlatinib‐resistant EML4‐ALK lung cancer cells in vitro model, to identify novel resistance mechanism. We found that activation of neuregulin‐1 (NRG1) and human epidermal growth factor receptor 3 (HER3) are largely responsible to resistance to lorlatinib, and pharmacological inhibition of HER3 with pan‐HER inhibitors genetic knockdown of HER3 with siRNA resensitized the lorlatinib cells to lorlatinib. The present study demonstrated a pivotal role of HER3 inhibition in lorlatinib‐resistant EML4‐ALK lung cancer cells caused by NRG1/HER3 activation.