Adrenomedullin2 stimulates progression of thyroid cancer in mice and humans under nutrient excess conditions

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dc.contributor.authorKim, Jung Taeko
dc.contributor.authorLim, Mi Aeko
dc.contributor.authorLee, Seong Eunko
dc.contributor.authorKim, Hyun Jungko
dc.contributor.authorKoh, Hyun Yongko
dc.contributor.authorLee, Jung Hoko
dc.contributor.authorJun, Sang Miko
dc.contributor.authorKim, Jin Manko
dc.contributor.authorKim, Kun Hoko
dc.contributor.authorShin, Hyo Shikko
dc.contributor.authorCho, Sun Wookko
dc.contributor.authorKim, Koon Soonko
dc.contributor.authorShong, Minhoko
dc.contributor.authorKoo, Bon Seokko
dc.contributor.authorKang, Yea Eunko
dc.date.accessioned2022-10-11T02:00:11Z-
dc.date.available2022-10-11T02:00:11Z-
dc.date.created2022-09-19-
dc.date.created2022-09-19-
dc.date.issued2022-11-
dc.identifier.citationJOURNAL OF PATHOLOGY, v.258, no.3, pp.264 - 277-
dc.identifier.issn0022-3417-
dc.identifier.urihttp://hdl.handle.net/10203/298913-
dc.description.abstractThyroid cancer is associated with genetic alterations, e.g. BRAF(V600E), which may cause carcinomatous changes in hormone-secreting epithelial cells. Epidemiological studies have shown that overnutrition is related to the development and progression of cancer. In this study, we attempted to identify the cell nonautonomous factor responsible for the progression of BRAF(V600E) thyroid cancer under overnutrition conditions. We developed a mouse model for inducible thyrocyte-specific activation of BRAF(V600E), which showed features similar to those of human papillary thyroid cancer. LSL-Braf(V600E);TgCreER(T2) showed thyroid tumour development in the entire thyroid, and the tumour showed more abnormal cellular features with mitochondrial abnormalities in mice fed a high-fat diet (HFD). Transcriptomics revealed that adrenomedullin2 (Adm2) was increased in LSL-Braf(V600E);TgCreER(T2) mice fed HFD. ADM2 was upregulated on the addition of a mitochondrial complex I inhibitor or palmitic acid with integrated stress response (ISR) in cancer cells. ADM2 stimulated protein kinase A and extracellular signal-regulated kinase in vitro. The knockdown of ADM2 suppressed the proliferation and migration of thyroid cancer cells. We searched The Cancer Genome Atlas and Genotype-Tissue Expression databases and found that increased ADM2 expression was associated with ISR and poor overall survival. Consistently, upregulated ADM2 expression in tumour cells and circulating ADM2 molecules were associated with aggressive clinicopathological parameters, including body mass index, in thyroid cancer patients. Collectively, we identified that ADM2 is released from cancer cells under mitochondrial stress resulting from overnutrition and acts as a secretory factor determining the progressive properties of thyroid cancer. (c) 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.-
dc.languageEnglish-
dc.publisherWILEY-
dc.titleAdrenomedullin2 stimulates progression of thyroid cancer in mice and humans under nutrient excess conditions-
dc.typeArticle-
dc.identifier.wosid000853015200001-
dc.identifier.scopusid2-s2.0-85137925711-
dc.type.rimsART-
dc.citation.volume258-
dc.citation.issue3-
dc.citation.beginningpage264-
dc.citation.endingpage277-
dc.citation.publicationnameJOURNAL OF PATHOLOGY-
dc.identifier.doi10.1002/path.5997-
dc.contributor.localauthorLee, Jung Ho-
dc.contributor.nonIdAuthorKim, Jung Tae-
dc.contributor.nonIdAuthorLim, Mi Ae-
dc.contributor.nonIdAuthorLee, Seong Eun-
dc.contributor.nonIdAuthorKim, Hyun Jung-
dc.contributor.nonIdAuthorJun, Sang Mi-
dc.contributor.nonIdAuthorKim, Jin Man-
dc.contributor.nonIdAuthorKim, Kun Ho-
dc.contributor.nonIdAuthorShin, Hyo Shik-
dc.contributor.nonIdAuthorCho, Sun Wook-
dc.contributor.nonIdAuthorKim, Koon Soon-
dc.contributor.nonIdAuthorShong, Minho-
dc.contributor.nonIdAuthorKoo, Bon Seok-
dc.contributor.nonIdAuthorKang, Yea Eun-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorthyroid cancer-
dc.subject.keywordAuthorobesity-
dc.subject.keywordAuthormitokine-
dc.subject.keywordAuthorADM2-
dc.subject.keywordAuthorcancer progression-
dc.subject.keywordAuthormitochondria-
dc.subject.keywordPlusDIET-INDUCED OBESITY-
dc.subject.keywordPlusADIPOSE-TISSUE-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusINTERMEDIN-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusPROTECTS-
dc.subject.keywordPlusSTRESS-
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