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Ultrastructural evidence of dimethylformamide‐induced differentiation of cultured human colon carcinoma cells increased expression of desmosomes
Author(s) -
Christensen Thomas G.,
Burke Bohdana,
Dexter Daniel L.,
Zamcheck Norman
Publication year - 1985
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19851001)56:7<1559::aid-cncr2820560716>3.0.co;2-t
Subject(s) - ultrastructure , cellular differentiation , pathology , carcinoma , cytoplasm , biology , chemistry , microbiology and biotechnology , medicine , biochemistry , gene
N,N‐dimethylformamide (DMF) induces differentiation of human colon carcinoma (DLD‐1) cells in culture and reduces their tumorigenicity in nude mice. The current investigation analyzed DLD‐1 (clone D) cells for ultrastructural evidence of differentiation. Examination of treated and untreated confluent monolayers by transmission electron microscopy revealed an occasional intracytoplasmic lumen indicative of adenocarcinoma. DMF‐treated cells showed no signs of a toxic reaction. Cytoplasmic organelles were essentially unchanged except for an increase in tonofilaments and associated desmosomes. The number of desmosomes per unit length of contiguous cell border increased almost sixfold in treated monolayers. No other type of cell junction was seen. The increased frequency of desmosomes in DMF‐treated cultures is significant because of the direct correlation known to exist between the number of desmosomes and degree of differentiation of some human carcinomas. Desmosomes serve as foci of cell adhesion and are reduced in number in some invasive tumors. Whether the supernumerary desmosomes in DMF‐treated cells contribute to the reduction in malignant behavior of these cells in vivo remains to be determined. Cancer 56: 1559‐1556, 1985.