Segal N H, Cohen R J, Haffejee Z, Savage N
Department of Anatomical Pathology, School of Pathology, South African Institute for Medical Research, Parktown.
Arch Pathol Lab Med. 1994 Jun;118(6):616-8.
Prostatic adenocarcinoma has a divergent response to androgen ablation and a varied long-term prognosis. BCL-2 is a proto-oncogene that prevents programmed cell death. Since androgen withdrawal induces apoptosis, it has been postulated that BCL-2 may play a role in androgen resistance. Neuroendocrine cells have been demonstrated in prostate cancer and have an adverse influence on long-term prognosis. This study demonstrates a proportional relationship between the tissue levels of BCL-2 and the neuroendocrine marker, neuron-specific enolase in 11 of 13 cases of primary prostate cancer. This relationship does not appear to exist in metastatic prostate cancer or in most nonprostate cancers. Direct immunohistochemical staining confirmed BCL-2 in six of the primary tumors, and these BCL-2-containing cells appeared to be intimately associated with tumor neuroendocrine cells.
前列腺腺癌对雄激素去除疗法反应不一,长期预后也各不相同。BCL-2是一种原癌基因,可阻止程序性细胞死亡。由于雄激素撤退会诱导细胞凋亡,因此有人推测BCL-2可能在雄激素抵抗中起作用。前列腺癌中已证实存在神经内分泌细胞,其对长期预后有不良影响。本研究表明,在13例原发性前列腺癌中的11例中,BCL-2的组织水平与神经内分泌标志物神经元特异性烯醇化酶之间存在比例关系。这种关系在转移性前列腺癌或大多数非前列腺癌中似乎不存在。直接免疫组织化学染色在6例原发性肿瘤中证实了BCL-2的存在,这些含有BCL-2的细胞似乎与肿瘤神经内分泌细胞密切相关。