Title

Laminin expression in colorectal carcinomas varying in degree of differentiation

UMMS Affiliation

Department of Cancer Biology

Publication Date

1987-12-01

Document Type

Article

Subjects

Animals; Basement Membrane; Carcinoma; Cell Line; Cell Transformation, Neoplastic; Colonic Neoplasms; Glycoproteins; Humans; Immunoenzyme Techniques; Laminin; Mice; Mice, Nude; Neoplasm Proteins; Neoplasm Transplantation; Precipitin Tests; Rectal Neoplasms; Tumor Cells, Cultured

Disciplines

Amino Acids, Peptides, and Proteins | Cancer Biology | Digestive System Diseases | Neoplasms

Abstract

We are studying the ability of colorectal carcinomas, which vary in degree of differentiation, to assemble a basement membrane and the relationship between differences in this ability and perturbations in laminin expression. For these studies, we are using human colorectal carcinoma cells grown both in vitro and in nude mice as well as tumors obtained at surgery. Immunoperoxidase staining of human tumors indicates that laminin is present in a defined basement membrane in moderately to well-differentiated tumors. This staining pattern is absent in poorly differentiated tumors. In these tumors, staining is discontinuous and sometimes observed intracellularly. The laminin synthesized by in vitro cells was immunoprecipitated and analyzed by acrylamide electrophoresis. Neither poorly nor well-differentiated carcinoma cells exhibit marked differences in the rate of synthesis of laminin. Differences are present in the rate at which newly synthesized laminin is secreted. These differences may result from alterations in posttranslational processing. Such alterations may contribute, along with other factors, to the inability of poorly differentiated tumors to make a basement membrane.

DOI of Published Version

10.1001/archsurg.1987.01400240118022

Source

Arch Surg. 1987 Dec;122(12):1470-4.

Journal/Book/Conference Title

Archives of surgery (Chicago, Ill. : 1960)

Related Resources

Link to Article in PubMed

PubMed ID

3318759

Link to Full Text

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