Bronzert D A, Pantazis P, Antoniades H N, Kasid A, Davidson N, Dickson R B, Lippman M E
Proc Natl Acad Sci U S A. 1987 Aug;84(16):5763-7. doi: 10.1073/pnas.84.16.5763.
We report that human breast cancer cells secrete a growth factor that is biologically and immunologically similar to platelet-derived growth factor (PDGF). Serum-free medium conditioned by estrogen-independent MDA-MB-231 or estrogen-dependent MCF-7 cells contains a mitogenic or "competence" activity that is capable of inducing incorporation of [3H]thymidine into quiescent Swiss 3T3 cells in the presence of platelet-poor plasma. In addition, the conditioned medium contains an activity that competes with 125I-labeled PDGF for binding to PDGF receptors on normal human fibroblasts. The secretion of PDGF-like activity by the hormone-responsive cell line MCF-7 is stimulated by 17 beta-estradiol. Like authentic PDGF, the PDGF-like activity produced by breast cancer cells is stable after acid and heat treatment (95 degrees C) and inhibited by reducing agents. The mitogenic activity comigrates with a material of approximately equal to 30 kDa on NaDodSO4/polyacrylamide gels. Immunoprecipitation with PDGF antiserum of proteins from metabolically labeled cell lysates and conditioned medium followed by analysis on nonreducing NaDodSO4/polyacrylamide gels identified proteins of 30 and 34 kDa. Upon reduction, the 30- and 34-kDa bands were converted to 15- and 16-kDa bands suggesting that the immunoprecipitated proteins were made up of two disulfide-linked polypeptides similar to PDGF. Hybridization studies with cDNA probes for the A chain of PDGF and the B chain of PDGF/SIS identified transcripts for both PDGF chains in the MCF-7 and MDA-MB-231 cells. The data summarized above provide conclusive evidence for the synthesis and hormonally regulated secretion of a PDGF-like mitogen by breast carcinoma cells. Production of a PDGF-like growth factor by breast cancer cell lines may be important in mediating paracrine stimulation of tumor growth.
我们报告称,人类乳腺癌细胞分泌一种生长因子,其在生物学和免疫学上与血小板衍生生长因子(PDGF)相似。由雌激素非依赖性MDA-MB-231细胞或雌激素依赖性MCF-7细胞条件培养的无血清培养基含有一种促有丝分裂或“能力”活性,在缺乏血小板的血浆存在下,这种活性能够诱导[3H]胸腺嘧啶掺入静止的瑞士3T3细胞。此外,条件培养基含有一种活性物质,它能与125I标记的PDGF竞争,以结合正常人成纤维细胞上的PDGF受体。激素反应性细胞系MCF-7分泌的PDGF样活性受到17β-雌二醇的刺激。与天然PDGF一样,乳腺癌细胞产生的PDGF样活性在酸和热处理(95℃)后稳定,并被还原剂抑制。促有丝分裂活性在NaDodSO4/聚丙烯酰胺凝胶上与大约30 kDa的物质共迁移。用PDGF抗血清对代谢标记的细胞裂解物和条件培养基中的蛋白质进行免疫沉淀,然后在非还原NaDodSO4/聚丙烯酰胺凝胶上进行分析,鉴定出30 kDa和34 kDa的蛋白质。还原后,30 kDa和34 kDa的条带转化为15 kDa和16 kDa的条带,表明免疫沉淀的蛋白质由两个类似于PDGF的二硫键连接的多肽组成。用PDGF A链和PDGF/SIS B链的cDNA探针进行杂交研究,在MCF-7和MDA-MB-231细胞中鉴定出了两种PDGF链的转录本。上述总结的数据为乳腺癌细胞合成和激素调节分泌PDGF样促有丝分裂原提供了确凿证据。乳腺癌细胞系产生PDGF样生长因子可能在介导肿瘤生长的旁分泌刺激中起重要作用。