Abstract Nestin (neuroepithelial stem cell protein) is a class VI intermediate filament protein which is transiently expressed in subsets of precursor cells of the peripheral and the central nervous system, muscle cells and other tissues during development. Upon differentiation, nestin expression becomes replaced by tissue-specific intermediate filament but it can be reinduced in the adult during pathological situations. In cancer, nestin was shown to promote tumor cell proliferation, migration, invasion, and angiogenesis. To determine the prevalence of nestin in cancer, nestin expression was analyzed by immunohistochemistry on tissue microarrays containing 5,917 samples from 107 different tumor types. Nestin positivity occurred in 749 (15.7%) of the 4,775 analyzable tumors, and was considered weak in 8.7%, moderate in 4.3%, and strong in 2.7% of cases. Of 107 tumor entities, 70 (65.4%) showed nestin expression in at least one case, and 22 (20.6%) included at least one case with strong nestin positivity. Highest rates tumors with nestin positivity occurred in pleomorphic adenoma of the parotid gland (100%), gastrointestinal stromal tumor (GIST; 93.8%), metastatic malignant melanoma (75.0%), pheochromocytoma (69.8%), leiomyosarcoma (47.4%), cholangiocarcinoma (40.6%), leiomyoma(40.0%), yolk sac tumor (34.1%), squamous cell carcinoma of the vagina (31.0%), the pharynx (27.3%), vulva (25.6%), anal canal (25.5%), oral cavity (24.7%), penis (19.4%), skin (14.7%), larynx (14.5%), cervix (10.8%), esophagus (9.5%), and the urinary bladder (9.5%), serous carcinoma of the ovary (26.7%), embryonal carcinoma of the testis (26.3%), adenocarcinoma of the cervix (26.1%), endometrioid endometrial carcinoma (22.1%), carcinosarcoma of the uterus(20.8%), pancreatic neuroendocrine tumor (20.7%), muscle-invasive urothelial carcinoma (18.3%), prostatic adenocarcinoma (17.2%), gastric adenocarcinoma of the intestinal type (16.2%), adenocarcinoma of the esophagus(15.1%), urothelial carcinoma of the kidney pelvis (14.3%), and in mucinous carcinoma of the ovary (14.3%). The largest cohort of tumors from one entity included 1,186 evaluable invasive breast cancers of no special type (NST). In these tumors, nestin staining was negative in 94.1%, weak in 3.9%, moderate in 1.3%, and strong in 0.8% of cases. A comparison with tumor phenotype revealed that detectable nestin expression was associated with advanced pT stage (p=0.0103), high grade of malignancy (p0.0001), absence of estrogen (p=0.0054) and progesterone (p=0.0051) receptor expression as well as with “triple negativity” (p=0.0028). The data from this study provide an overview of nestin expression in human cancer and demonstrate that increased nestin levels can occur in many different tumor entities. At least in breast cancer NST, nestin positivity goes along with increased cancer aggressiveness. Citation Format: Clara von Bargen, Muriel Torzewski, Fiete Gehrisch, Anne Menz, Florian Lutz, Viktoria Chirico, Florian Viehweger, David Dum, Ria Schlichter, Andrea Hinsch, Christoph Fraune, Chrisitan Bernreuther, Seyma Büyücek, Martina Kluth, Claudia Hube-Magg, Georgia Makrypidi-Fraune, Nina Schraps, Katharina Möller, Andreas M Luebke, Patrick Lekok, Guido Sauter, Maximilian Lennartz, Till Clauditz, Andreas H Marx, Ronald Simon, Eike Burandt, Natalia Gorbokon, Maria Chrisitna Tsourlakis, Sarah Minner, Till Krech, Morton Freytag, Viktor Reiswich, Stefan Steurer. Nestin expression is prevalent but highly variable in human cancer: A tissue microarray study involving 5,917 cancers from 107 tumor entities 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 1105.
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Clara von Bargen
Muriel Torzewski
Fiete Gehrisch
Cancer Research
Universität Hamburg
University Medical Center Hamburg-Eppendorf
Klinikum Fürth
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Bargen et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fd8ea79560c99a0a3aef — DOI: https://doi.org/10.1158/1538-7445.am2026-1105