TY - JOUR
T1 - Towards a new "stromal-based" classification system for human breast cancer prognosis and therapy
AU - Witkiewicz, Agnieszka K.
AU - Casimiro, Mathew C.
AU - Dasgupta, Abhijit
AU - Mercier, Isabelle
AU - Wang, Chenguang
AU - Bonuccelli, Gloria
AU - Jasmin, Jean François
AU - Frank, Philippe G.
AU - Pestell, Richard G.
AU - Kleer, Celina G.
AU - Sotgia, Federica
AU - Lisanti, Michael P.
N1 - Funding Information:
supported by a Career Catalyst Award from the Susan G. Komen Breast Cancer Foundation. C.G.K. was supported by NIH/NCI grants (R01-CA-090876 and R01-CA-107469) and a grant from the Avon Foundation. R.G.P. was supported by grants from the NIH/NCI (R01-CA-70896, R01-CA-75503, R01-CA-86072 and R01-CA-107382) and the Dr. Ralph and Marian C. Falk Medical Research Trust. The Kimmel Cancer Center was supported by the NIH/NCI Cancer Center Core grant P30-CA-56036 (to R.G.P.).
Funding Information:
This project is funded, in part, under a grant with the Pennsylvania Department of Health (to M.P.L.). The Department specifically disclaims responsibility for any analyses, interpretations or conclusions.
Funding Information:
M.P.L. and his laboratory were supported by grants from the NIH/NCI (R01-CA-80250; R01-CA-098779; R01-CA-120876), the American Association for Cancer Research (AACR), the Susan G. Komen Breast Cancer Foundation, and the Department of Defense-Breast Cancer Research Program (Synergistic Idea Award). A.K.W. was supported by a Young Investigator Award from Breast Cancer Alliance, Inc., and a Susan G. Komen Career Catalyst Grant. F.S. was supported by grants from the Elsa U. Pardee Foundation, the W.W. Smith Charitable Trust, the Breast Cancer Alliance, and a Research Scholar Grant from the American Cancer Society (ACS). I.M. was supported by a Post-doctoral Fellowship from the Susan G. Komen Breast Cancer Foundation. P.G.F. was supported by a grant from the W.W. Smith Charitable Trust, and a Career Catalyst Award from the Susan G. Komen Breast Cancer Foundation. J.F.J. was
PY - 2009/6/1
Y1 - 2009/6/1
N2 - Here, we discuss recent evidence that an absence of stromal Cav-1 expression in human breast cancers is a powerful single independent predictor of early disease recurrence, metastasis and poor clinical outcome. These findings have now been validated in two independent patient populations. Importantly, the predictive value of stromal Cav-1 is independent of epithelial marker status, making stromal Cav-1 a new "universal" or "widely- applicable" breast cancer prognostic marker. We propose based on the expression of stromal Cav-1, that breast cancer patients could be stratified into high-risk and low-risk groups. High-risk patients showing an absence of stromal Cav-1 should be offered more aggressive therapies, such as anti-angiogenic approaches, in addition to the standard therapy regimens. Mechanistically, loss of stromal Cav-1 is a surrogate biomarker for increased cell cycle progression, growth factor secretion, "stemness", and angiogenic potential in the tumor microenvironment. Since almost all cancers develop within the context of a stromal microenvironment, this new stromal classification system may be broadly applicable to other epithelial and non-epithelial cancer subtypes, as well as "pre-malignant" lesions (carcinoma in situ).
AB - Here, we discuss recent evidence that an absence of stromal Cav-1 expression in human breast cancers is a powerful single independent predictor of early disease recurrence, metastasis and poor clinical outcome. These findings have now been validated in two independent patient populations. Importantly, the predictive value of stromal Cav-1 is independent of epithelial marker status, making stromal Cav-1 a new "universal" or "widely- applicable" breast cancer prognostic marker. We propose based on the expression of stromal Cav-1, that breast cancer patients could be stratified into high-risk and low-risk groups. High-risk patients showing an absence of stromal Cav-1 should be offered more aggressive therapies, such as anti-angiogenic approaches, in addition to the standard therapy regimens. Mechanistically, loss of stromal Cav-1 is a surrogate biomarker for increased cell cycle progression, growth factor secretion, "stemness", and angiogenic potential in the tumor microenvironment. Since almost all cancers develop within the context of a stromal microenvironment, this new stromal classification system may be broadly applicable to other epithelial and non-epithelial cancer subtypes, as well as "pre-malignant" lesions (carcinoma in situ).
KW - Biomarkers
KW - Breast cancer
KW - Cancer-associated fibroblasts
KW - Caveolin-1
KW - Prognosis
KW - Stroma
KW - Treatment stratification
UR - http://www.scopus.com/inward/record.url?scp=66749147690&partnerID=8YFLogxK
U2 - 10.4161/cc.8.11.8544
DO - 10.4161/cc.8.11.8544
M3 - Review article
C2 - 19448435
AN - SCOPUS:66749147690
SN - 1538-4101
VL - 8
SP - 1654
EP - 1658
JO - Cell Cycle
JF - Cell Cycle
IS - 11
ER -