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Stromal type I collagen in breast cancer : correlation to prognostic biomarkers and prediction of chemotherapy response

Jansson, Malin, 1978- (author)
Umeå universitet,Kirurgi
Lindberg, Jessica (author)
Umeå universitet,Kirurgi
Rask, Gunilla (author)
Umeå universitet,Patologi
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Svensson, Johan, 1978- (author)
Umeå universitet,Statistik,Kirurgi
Billing, Ola, 1981- (author)
Umeå universitet,Kirurgi
Nazemroaya, Anoosheh (author)
Umeå universitet,Patologi
Berglund, Anette, 1960- (author)
Umeå universitet,Kirurgi
Wärnberg, Fredrik (author)
Department of Surgery, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden
Sund, Malin (author)
Umeå universitet,Kirurgi,Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
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 (creator_code:org_t)
Elsevier, 2024
2024
English.
In: Clinical Breast Cancer. - : Elsevier. - 1526-8209 .- 1938-0666.
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Introduction: Fibrillar collagens accumulate in the breast cancer stroma and appear as poorly defined spiculated masses in mammography imaging. The prognostic value of tissue type I collagen remains elusive in treatment-naïve and chemotherapy-treated breast cancer patients. Here, type I collagen mRNA and protein expression were analysed in 2 large independent breast cancer cohorts. Levels were related to clinicopathological parameters, prognostic biomarkers, and outcome.Method: COL1A1 mRNA expression was analysed in 2509 patients with breast cancer obtained from the cBioPortal database. Type I collagen protein expression was studied by immunohistochemistry in 1395 women diagnosed with early invasive breast cancer.Results: Low COL1A1 mRNA and protein levels correlated with poor prognosis features, such as hormone receptor negativity, high histological grade, triple-negative subtype, node positivity, and tumour size. In unadjusted analysis, high stromal type I collagen protein expression was associated with improved overall survival (OS) (HR = 0.78, 95% CI = 0.61-0.99, p = .043) and trended towards improved breast cancer–specific survival (BCSS) (HR = 0.65, 95% CI = 0.42-1.01, P = 0.053), although these findings were lost after adjustment for other clinical variables. In unadjusted analysis, high expression of type I collagen was associated with better OS (HR = 0.70, 95% CI = 0.55-0.90, P = .006) and BCSS (HR = 0.55, 95% CI = 0.34-0.88, P = .014) among patients not receiving chemotherapy. Strikingly, the opposite was observed among patients receiving chemotherapy. There, high expression of type I collagen was instead associated with worse OS (HR = 1.83, 95% CI = 0.65-5.14, P = .25) and BCSS (HR = 1.72, 95% CI = 0.54-5.50, P = .357).Conclusion: Low stromal type I collagen mRNA and protein expression are associated with unfavourable tumour characteristics in breast cancer. Stromal type I collagen might predict chemotherapy response.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Breast cancer
Chemotherapy response
Extracellular matrix
Tumour microenvironment
Type I collagen

Publication and Content Type

ref (subject category)
art (subject category)

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