S100A10 has a critical regulatory function in mammary tumor growth and metastasis: Insights using MMTV-PyMT oncomice and clinical patient sample analysis

Alamelu G. Bharadwaj, Margaret L. Dahn, Rong Zong Liu, Patricia Colp, Lynn N. Thomas, Ryan W. Holloway, Paola A. Marignani, Catherine K.L. Too, Penelope J. Barnes, Roseline Godbout, Paola Marcato, David M. Waisman

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

10 Citas (Scopus)

Resumen

S100A10 (p11) is a plasminogen receptor that regulates cellular plasmin generation by cancer cells. In the current study, we used the MMTV-PyMT mouse breast cancer model, patient tumor microarray, and immunohistochemical (IHC) analysis to investigate the role of p11 in oncogenesis. The genetic deletion of p11 resulted in significantly decreased tumor onset, growth rate, and spontaneous pulmonary metastatic burden in the PyMT/p11-KO (knock-out) mice. This phenotype was accompanied by substantial reduction in Ki67 positivity, macrophage infiltration, decreased vascular density in the primary tumors, and decrease in invasive carcinoma and pulmonary metastasis. Surprisingly, IHC analysis of wild-type MMTV-PyMT mice failed to detect p11 expression in the tumors or metastatic tumor cells and loss of p11 did not decrease plasmin generation in the PyMT tumors and cells. Furthermore, tumor cells expressing p11 displayed dramatically reduced lung metastasis when injected into p11-depleted mice, further strengthening the stromal role of p11 in tumor growth and metastasis. Transcriptome analysis of the PyMT tumors from p11-KO mice showed marked reduction in genes such as Areg, Muc1, and S100a8 involved in breast cancer development, progression, and inflammation. The PyMT/p11-KO tumors displayed a remarkable increase in inflammatory cytokines such as interleukin (Il)-6, Il-10, and interferon (Ifn)-γ. Gene expression profiling and IHC of primary breast cancer samples showed that p11 mRNA and protein levels were significantly higher in tumor tissues compared to normal mammary tissue. P11 mRNA expression was significantly associated with poor patient prognosis and significantly elevated in high grade, triple negative (TN) tumors, and tumors with high proliferative index. This is the first study examining the crucial role of p11 in breast tumor development and metastasis, thus emphasizing its potential as a diagnostic and prognostic biomarker in breast cancer.

Idioma originalEnglish
Número de artículo3673
Páginas (desde-hasta)1-22
Número de páginas22
PublicaciónCancers
Volumen12
N.º12
DOI
EstadoPublished - dic. 2020

Nota bibliográfica

Funding Information:
Funding: A.G.B is supported by a trainee award from the Beatrice Hunter Cancer Research Institute with funds provided by the Harvey Graham Cancer Research Fund as part of The Terry Fox Strategic Health Research Training Program in Cancer Research at CIHR. M.L.D. is supported by CGS-D award from the CIHR, a Nova Scotia Health Research Foundation studentship, a Nova Scotia Research and Innovation Graduate scholarship, a Beatrice Hunter Cancer Research Institute Cancer Research Training Program studentship, and a Killam Laureate scholarship. P.A.M. is supported by funding from Dalhousie Medical Research Foundation (DMRF) and Breast Cancer Society of Canada (BCSC). R.G. is supported by a grant from Canadian Cancer Research Institute (grant No. 705455). C.K.L.T. is supported Canadian Breast Cancer Foundation/Atlantic, Canadian Cancer Society and Breast Cancer Society of Canada, QEII Foundation, Beatrice Hunter Cancer Research Institute, P.J.B. is supported by Breast Cancer Society of Canada, QEII Foundation, Beatrice Hunter Cancer Research Institute. P.M. is supported by CIHR, PJT 162313. D.M.W. and this research is supported by a grant from the CIHR.

Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.

ASJC Scopus Subject Areas

  • Oncology
  • Cancer Research

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