Abstract 4761: Investigation of the role of N-MYC in lung neuroendocrine carcinoma

Abstract Small cell lung cancer and large cell neuroendocrine carcinoma are classified as high-grade neuroendocrine tumors of the lung, representing extremely aggressive, life-threatening cancers with limited treatment options among various lung cancers. In these cancers, amplification of MYC family transcription factors: c-MYC, L-MYC and N-MYC is found to be mutually exclusive and overall account for ∼20%. In addition, recent studies have reported that L-MYC and c-MYC control lineage plasticity across molecular subtypes of small cell lung cancer defined by lineage-specific transcription factors such as ASCL-1 and NEUROD-1. Compared with L-MYC and c-MYC, the role of N-MYC, a lineage factor highly expressed in several tumors derived from neural cell lineages and a subset of neuroendocrine lung cancers, have not been described clearly. In this study, we aimed to investigate the role of N-MYC as a lineage-specific factors in neuroendocrine lung cancers. First, we investigated N-MYC binding profiles in N-MYC-high neuroendocrine lung cancer cell lines and found that genes related to neural cell differentiation were enriched in genes near N-MYC bound regions. Next, examination of genome-wide Myc-accessible regions in neuroendocrine lung cancer cell lines revealed that a fraction of peaks that overlapped between N-MYC- and c-MYC-classified cells, suggesting common functional binding of N-MYC and c-MYC. When we overexpressed N-MYC in L-MYC- or c-MYC-classified cells, expression profiles of the neuroendocrine lineage factors did not change, which was different from the previous findings on the relationships between L-MYC and c-MYC. Our findings suggest that N-MYC regulates distinct transcriptional program among the MYC family members although N-MYC and c-MYC share common binding profile. Citation Format: Hiroki Yamamoto, Takashi Sato, Yuri Yagami, Ryosuke Inoue, Hiromi Matsuo, Hideo Watanabe, Naoki Katsuhiko. Investigation of the role of N-MYC in lung neuroendocrine carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4761.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-4761
Primary Topic
Lung Cancer Research Studies
Type
article
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article

Abstract 4761: Investigation of the role of N-MYC in lung neuroendocrine carcinoma

Yuri Yagami, Naoki Katsuhiko, Hideo Watanabe, Ryosuke Inoue et al.
Cancer Research
Lung Cancer Research Studies
article

Abstract 4761: Investigation of the role of N-MYC in lung neuroendocrine carcinoma

Yuri Yagami, Naoki Katsuhiko, Hideo Watanabe, Ryosuke Inoue, Hiroki Yamamoto, Takashi Sato, Hiromi Matsuo
article en

Abstract

Abstract Small cell lung cancer and large cell neuroendocrine carcinoma are classified as high-grade neuroendocrine tumors of the lung, representing extremely aggressive, life-threatening cancers with limited treatment options among various lung cancers. In these cancers, amplification of MYC family transcription factors: c-MYC, L-MYC and N-MYC is found to be mutually exclusive and overall account for ∼20%. In addition, recent studies have reported that L-MYC and c-MYC control lineage plasticity across molecular subtypes of small cell lung cancer defined by lineage-specific transcription factors such as ASCL-1 and NEUROD-1. Compared with L-MYC and c-MYC, the role of N-MYC, a lineage factor highly expressed in several tumors derived from neural cell lineages and a subset of neuroendocrine lung cancers, have not been described clearly. In this study, we aimed to investigate the role of N-MYC as a lineage-specific factors in neuroendocrine lung cancers. First, we investigated N-MYC binding profiles in N-MYC-high neuroendocrine lung cancer cell lines and found that genes related to neural cell differentiation were enriched in genes near N-MYC bound regions. Next, examination of genome-wide Myc-accessible regions in neuroendocrine lung cancer cell lines revealed that a fraction of peaks that overlapped between N-MYC- and c-MYC-classified cells, suggesting common functional binding of N-MYC and c-MYC. When we overexpressed N-MYC in L-MYC- or c-MYC-classified cells, expression profiles of the neuroendocrine lineage factors did not change, which was different from the previous findings on the relationships between L-MYC and c-MYC. Our findings suggest that N-MYC regulates distinct transcriptional program among the MYC family members although N-MYC and c-MYC share common binding profile. Citation Format: Hiroki Yamamoto, Takashi Sato, Yuri Yagami, Ryosuke Inoue, Hiromi Matsuo, Hideo Watanabe, Naoki Katsuhiko. Investigation of the role of N-MYC in lung neuroendocrine carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4761.

Cancer ResearchVol. 86(7_Supplement)
Kitasato University (JP), Icahn School of Medicine at Mount Sinai (US)
Good health and well-being
Openalex Percentile: Top 9%
Lung Cancer Research Studies
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