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Title: Tuft cell-like carcinomas: novel cancer subsets present in multiple organs sharing a unique gene expression signature
Authors: Yamada, Yosuke  KAKEN_id  orcid https://orcid.org/0000-0001-7952-2706 (unconfirmed)
Bohnenberger, Hanibal
Kriegsmann, Mark
Kriegsmann, Katharina
Sinn, Peter
Goto, Norihiro
Nakanishi, Yuki  kyouindb  KAKEN_id
Seno, Hiroshi  kyouindb  KAKEN_id
Chigusa, Yoshitsugu  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-9629-5912 (unconfirmed)
Fujimoto, Masakazu  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0575-6507 (unconfirmed)
Minamiguchi, Sachiko  KAKEN_id  orcid https://orcid.org/0000-0002-5800-6769 (unconfirmed)
Haga, Hironori  kyouindb  KAKEN_id
Simon, Ronald
Sauter, Guido
Ströbel, Philipp
Marx, Alexander
Author's alias: 山田, 洋介
後藤, 規弘
中西, 祐貴
妹尾, 浩
千草, 義継
藤本, 正数
南口, 早智子
羽賀, 博典
Keywords: Oncogenes
Issue Date: 9-Nov-2022
Publisher: Springer Nature
Journal title: British Journal of Cancer
Volume: 127
Issue: 10
Start page: 1876
End page: 1885
Abstract: [Background] Tuft cells are chemosensory epithelial cells playing a role in innate immunity. Recent studies revealed cancers with a tuft cell-like gene expression signature in the thorax. We wondered whether this signature might also occur in extrathoracic cancers. [Methods] We examined mRNA expression of tuft cell markers (POU2F3, GFI1B, TRPM5, SOX9, CHAT, and AVIL) in 19 different types of cancers in multiple extrathoracic organs with The Cancer Genome Atlas (TCGA) (N = 6322). Four different extrathoracic cancers in our local archives (N = 909) were analysed by immunohistochemistry. [Results] Twenty-two (0.35%) extrathoracic tumours with co-expression of POU2F3 and other tuft cell markers were identified in various TCGA datasets. Twelve of the 22 “tuft cell-like tumours” shared poor differentiation and a gene expression pattern, including KIT, anti-apoptotic BCL2, and ionocyte-associated genes. In our archival cases, eleven (1.21%) tumours co-expressing POU2F3, KIT, and BCL2 on immunohistochemistry, i.e., were presumable tuft cell-like cancers. In three among five TCGA cohorts, the tuft cell-like cancer subsets expressed SLFN11, a promising biomarker of PARP inhibitor susceptibility. [Conclusions] Tuft cell-like carcinomas form distinct subsets in cancers of many organs. It appears warranted to investigate their shared gene expression signature as a predictive biomarker for novel therapeutic strategies.
Rights: This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1038/s41416-022-01957-6.
The full-text file will be made open to the public on 23 February 2023 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.
This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
URI: http://hdl.handle.net/2433/277100
DOI(Published Version): 10.1038/s41416-022-01957-6
PubMed ID: 35999270
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