| Literature DB >> 27923833 |
Sijana H Dzinic1,2, M Margarida Bernardo1,2, Xiaohua Li1,2, Rodrigo Fernandez-Valdivia1,2, Ye-Shih Ho3, Qing-Sheng Mi2,4,5, Sudeshna Bandyopadhyay1,2, Fulvio Lonardo1,2, Semir Vranic6, Daniel S M Oliveira1,2,7, R Daniel Bonfil1,2,7,8, Gregory Dyson2,8, Kang Chen2,4,7,8,9,10, Almasa Omerovic1,2, Xiujie Sheng11, Xiang Han12, Dinghong Wu4,5, Xinling Bi4,5, Dzenana Cabaravdic1,2, Una Jakupovic1,2, Marian Wahba13, Aaron Pang1,2, Deanna Harajli1,2, Wael A Sakr1,2, Shijie Sheng14,2,8.
Abstract
Maspin (SerpinB5) is an epithelial-specific tumor suppressor gene product that displays context-dependent cellular functions. Maspin-deficient mouse models created to date have not definitively established maspin functions critical for cancer suppression. In this study, we generated a mouse strain in which exon 4 of the Maspin gene was deleted, confirming its essential role in development but also enabling a breeding scheme to bypass embryonic lethality. Phenotypic characterization of this viable strain established that maspin deficiency was associated with a reduction in maximum body weight and a variety of context-dependent epithelial abnormalities. Specifically, maspin-deficient mice exhibited pulmonary adenocarcinoma, myoepithelial hyperplasia of the mammary gland, hyperplasia of luminal cells of dorsolateral and anterior prostate, and atrophy of luminal cells of ventral prostate and stratum spinosum of epidermis. These cancer phenotypes were accompanied by increased inflammatory stroma. These mice also displayed the autoimmune disorder alopecia aerate. Overall, our findings defined context-specific tumor suppressor roles for maspin in a clinically relevant model to study maspin functions in cancer and other pathologies. Cancer Res; 77(4); 886-96. ©2017 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27923833 PMCID: PMC5313336 DOI: 10.1158/0008-5472.CAN-16-2219
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701