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Relation of endocrine‐paracrine cells to cell proliferation in normal, hyperplastic, and neoplastic human prostate
Author(s) -
Bonkhoff Helmut,
Wernert Nicolas,
Dhom Georg,
Remberger Klaus
Publication year - 1991
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.2990190202
Subject(s) - endocrine system , paracrine signalling , prostate , adenocarcinoma , pathology , biology , enteroendocrine cell , malignancy , cancer research , endocrinology , medicine , hormone , cancer , receptor
The relative distribution pattern of the pan‐endocrine marker Chromogranin A (Chr A) and the proliferation‐associated Ki‐67 antigen was investigated in 20 prospectively sampled prostatectomy specimens. In cryostat sections, the Chr A immunoreactivity showed evidence of endocrine differentiation in all 15 prostatic adenocarcinomas. Nine tumors displayed a weak, 5 a moderate, and 1 adenocarcinoma a strong endocrine differentiation. These findings highlight the importance of endocrine differentiation in prostate malignancy that histologically resembles ordinary adenocarcinomas. The simultaneous demonstration of Ki‐67 and Chr A revealed that in normal, hyperplastic, and neoplastic prostate tissue Chr A‐positive cells were preferentially situated in proximity to Ki‐67‐labeled cells. This relative distribution pattern of both markers may indicate that endocrine cells are involved in controlling cell proliferation through a paracrine hormonal mechanism. However, an obvious correlation was not found between the degree of endocrine differentiation and proliferative activity in prostatic adenocarcinomas. Furthermore, a coexpression of Ki‐67 and Chr A in the same (tumor) cells was not observed suggesting that the endocrine phenotype is only expressed in the G 0 phase of the cell cycle as well as in normal, hyperplastic, and neoplastic conditions.