Evidence map›Paper›PMID 41847153›Full record

ArticleJTO clinical and research reports2026

Brief Report: Androgen Receptor Expression Is Associated With Male Predominance in Thymic Neuroendocrine Neoplasms.

Christopher S Nabel, Chad B Sussman, Charles A Whittaker, Vincent L Butty, Jennifer L Peterson, Haley K Martin, Abner Louissaint, Eva Bru-Tari, Simona Chera, Azra H Ligon and 3 more

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Article in JTO clinical and research reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Christopher S NabelMass General Brigham Cancer Institute, Boston, Massachusetts.
Chad B SussmanHarvard Medical School, Boston, Massachusetts.
Charles A WhittakerKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Vincent L ButtyKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Jennifer L PetersonMass General Brigham Cancer Institute, Boston, Massachusetts.
Haley K MartinDepartment of Pathology, Massachusetts General Brigham, Boston, Massachusetts.
Abner LouissaintHarvard Medical School, Boston, Massachusetts.
Eva Bru-TariUniversity of Geneva, Geneva, Switzerland.
Simona CheraUniversity of Geneva, Geneva, Switzerland.
Azra H LigonHarvard Medical School, Boston, Massachusetts.
Beow Y YeapMass General Brigham Cancer Institute, Boston, Massachusetts.
Pedro L HerreraUniversity of Geneva, Geneva, Switzerland.
Yin P HungHarvard Medical School, Boston, Massachusetts.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Neuroendocrine neoplasms represent a rare and poorly understood collection of malignancies. A better understanding of their biology is needed to improve treatment options. Male predominance to the incidence of neuroendocrine neoplasms of the thymus suggests a biological basis for this observation. Methods: This single-institution, retrospective cohort study evaluated androgen receptor (AR) expression and other clinicopathologic features in thymic neuroendocrine neoplasms compared with thymic epithelial tumors and neuroendocrine neoplasms of other sites. Expression of neuroendocrine and prostate markers was also assessed. For further molecular characterization, copy number analysis of AR and other relevant genes was assessed by single nucleotide polymorphism array. Last, analysis of single genes and thymic epithelial gene sets was performed using published thymic tumor transcriptomes. Results: A cohort was assembled from 17 patients with neuroendocrine malignancies of primary thymic origin with assessable tissue for immunohistochemical analysis. The cohort was predominantly male (12 males, five females). Immunohistochemical analysis of the AR demonstrated positive staining in nine cases, all of which were male. Compared with thymic neuroendocrine neoplasms, AR expression is considerably less frequent in thymomas, thymic carcinoma, and neuroendocrine neoplasms of other sites of origin. No relevant copy number changes in the AR were identified. Further molecular characterization revealed expression of ASCL1 and limited expression of common prostate lineage and differentiation markers within our cohort, including thymic neuroendocrine epithelial gene set enrichment in published transcriptomes of thymic neuroendocrine neoplasms. Conclusion: The AR is expressed in a considerable fraction of thymic neuroendocrine neoplasms and is associated with male predominance. This observation has implications for investigation of androgen deprivation and receptor blockade.

Indexed as

Androgen receptorMolecular characterizationNeuroendocrine neoplasmsThymic epithelial tumorsThymic neuroendocrine tumor

Identifiers

PMID41847153
PMCPMC12989837

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