» Articles » PMID: 7962040

Tumour Vascularity and Basement Membrane Structure in Breast Cancer As Related to Tumour Histology and Prognosis

Overview
Specialty Oncology
Date 1994 Jan 1
PMID 7962040
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

A series of 202 breast cancer biopsy specimens were analysed immunohistochemically for collagen IV to demonstrate basement membrane (BM) structures and blood vessels within tumour tissue. Integrity of the BM was graded into four categories and the number of vascular channels per square millimetre of tumour tissue were counted. Defective BM structures were significantly related to high grade, lack of tubule formation, invasive disease, high S-phase fraction and variability in nuclear size and shape. High vascular channel density was related to poor tumour differentiation and a high proliferation rate of cancer cells as well as to the absence of tubule formation, inconspicuous intraductal growth and low progesterone receptor content. High vascular density and defective BM structures were signs of poor prognosis and short recurrence-free survival in the entire cohort and also in local tumours. In multivariate analysis, the vascular density had independent prognostic value, as did the diameter, axillary lymph node status and mitotic rate. The counting of vascular channels within the tumour provides additional prognostic information in breast cancer, in contrast to analysis of the BM integrity which shows hardly any prognostic information additional to that provided by the special histological features, e.g. tubule formation and intraductal growth pattern.

Citing Articles

Deep learning identification of stiffness markers in breast cancer.

Sneider A, Kiemen A, Kim J, Wu P, Habibi M, White M Biomaterials. 2022; 285:121540.

PMID: 35537336 PMC: 9873266. DOI: 10.1016/j.biomaterials.2022.121540.


Saturation transfer properties of tumour xenografts derived from prostate cancer cell lines 22Rv1 and DU145.

Tan Z, Lam W, Oakden W, Murray L, Koletar M, Liu S Sci Rep. 2020; 10(1):21315.

PMID: 33277574 PMC: 7718243. DOI: 10.1038/s41598-020-78353-8.


The Basement Membrane in a 3D Breast Acini Model Modulates Delivery and Anti-Proliferative Effects of Liposomal Anthracyclines.

Wiedenhoeft T, Braun T, Springer R, Teske M, Noetzel E, Merkel R Pharmaceuticals (Basel). 2020; 13(9).

PMID: 32961780 PMC: 7558514. DOI: 10.3390/ph13090256.


Visualization of basement membranes in normal breast and breast cancer tissues using multiphoton microscopy.

Wu X, Chen G, Qiu J, Lu J, Zhu W, Chen J Oncol Lett. 2016; 11(6):3785-3789.

PMID: 27313695 PMC: 4888276. DOI: 10.3892/ol.2016.4472.


Dormant but migratory tumour cells in desmoplastic stroma of invasive ductal carcinomas.

Raviraj V, Zhang H, Chien H, Cole L, Thompson E, Soon L Clin Exp Metastasis. 2012; 29(3):273-92.

PMID: 22271313 DOI: 10.1007/s10585-011-9450-4.


References
1.
Barnhill R, Levy M . Regressing thin cutaneous malignant melanomas (< or = 1.0 mm) are associated with angiogenesis. Am J Pathol. 1993; 143(1):99-104. PMC: 1886944. View

2.
Lah T, Strukelj B, Pungercar J, Barlic-Maganja D, Drobnic-Kosorok M, Kastelic L . Stefins and lysosomal cathepsins B, L and D in human breast carcinoma. Int J Cancer. 1992; 50(1):36-44. DOI: 10.1002/ijc.2910500109. View

3.
Bosari S, Lee A, DeLellis R, Wiley B, Heatley G, Silverman M . Microvessel quantitation and prognosis in invasive breast carcinoma. Hum Pathol. 1992; 23(7):755-61. DOI: 10.1016/0046-8177(92)90344-3. View

4.
Lipponen P, Aaltomaa S, Eskelinen M, Kosma V, Marin S, Syrjanen K . The changing importance of prognostic factors in breast cancer during long-term follow-up. Int J Cancer. 1992; 51(5):698-702. DOI: 10.1002/ijc.2910510506. View

5.
Raymond W, Leong A . Assessment of invasion in breast lesions using antibodies to basement membrane components and myoepithelial cells. Pathology. 1991; 23(4):291-7. DOI: 10.3109/00313029109063591. View