Lewko W M, Liotta L A, Wicha M S, Vonderhaar B K, Kidwell W R
Cancer Res. 1981 Jul;41(7):2855-62.
The growth of primary N-nitrosomethylurea-induced rat mammary tumors was depressed by cis-hydroxyproline (CHP). This growth arrest appeared to be related to the ability of CHP to inhibit the deposition of basement membrane collagen as based on the following observations: (a) in vitro and in vivo, tumor cells synthesized type IV collagen, the collagen uniquely localized in basement membranes; (b) in vitro, the inhibition of tumor cell growth was preceded by a specific decrease in collagen accumulation with no effect on non-collagen protein synthesis; (c) a transplantable N-nitrosomethylurea-induced rat mammary tumor accumulated no type IV collagen as determined by polyacrylamide gel electrophoresis and indirect immunofluorescence. The growth of this tumor was not influenced by CHP; (d) an established human mammary tumor cell line, MCF-7, did not accumulate type IV collagen and was not inhibited by CHP. At the doses which effectively blocked the growth of primary N-nitrosomethylurea-induced mammary tumors, CHP and no toxic effects, and serum prolactin levels were not altered. The inhibitory effect was thus apparently due to the direct action of CHP upon the accumulation of collagen in cells which required type IV collagen production for continued growth.
顺式羟脯氨酸(CHP)可抑制N-亚硝基甲基脲诱导的大鼠原发性乳腺肿瘤的生长。基于以下观察结果,这种生长停滞似乎与CHP抑制基底膜胶原蛋白沉积的能力有关:(a)在体外和体内,肿瘤细胞合成IV型胶原蛋白,这种胶原蛋白独特地定位于基底膜中;(b)在体外,肿瘤细胞生长受到抑制之前,胶原蛋白积累会特异性减少,而对非胶原蛋白合成没有影响;(c)通过聚丙烯酰胺凝胶电泳和间接免疫荧光测定,可移植的N-亚硝基甲基脲诱导的大鼠乳腺肿瘤不积累IV型胶原蛋白。该肿瘤的生长不受CHP影响;(d)已建立的人乳腺肿瘤细胞系MCF-7不积累IV型胶原蛋白,也不受CHP抑制。在有效阻断N-亚硝基甲基脲诱导的原发性乳腺肿瘤生长的剂量下,CHP没有毒性作用,血清催乳素水平也未改变。因此,这种抑制作用显然是由于CHP对那些需要产生IV型胶原蛋白以持续生长的细胞中胶原蛋白积累的直接作用。