al-Mondhiry H, Wallin R
Department of Medicine, College of Medicine, Pennsylvania State University, Milton S. Hershey Medical Center, Hershey, PA.
Thromb Haemost. 1989 Sep 29;62(2):661-6.
The observation that warfarin inhibits the growth and metastasis of certain types of clinical and experimental tumors suggests a role for vitamin K in tumor biology. We have investigated synthesis of vitamin K-dependent proteins in four malignant (lung epidermoid carcinoma, melanoma, colon adenocarcinoma, and breast adenocarcinoma) and three normal (colon epithelium, breast epithelium, and fibroblasts) cell lines of human origin grown in tissue cultures. Our results show the following: 1) Vitamin K-dependent carboxylase activity is present in all of the malignant and normal cell lines studied. 2) The malignant as well as normal cell lines synthesize a family of vitamin K-dependent proteins. Microsomal precursors of these proteins with apparent molecular mass of 74, 62, and 34 kDa are common to all malignant and normal cell lines whereas precursors of higher and lower molecular mass seem to be synthesized by some but not all tumor cell lines. 3) The 74 kDa precursor synthesized by colon carcinoma and breast carcinoma was positively identified as a precursor of protein S.
华法林可抑制某些临床及实验性肿瘤的生长和转移,这一观察结果提示维生素K在肿瘤生物学中具有一定作用。我们研究了在组织培养中生长的四种人类来源的恶性细胞系(肺表皮样癌、黑色素瘤、结肠腺癌和乳腺腺癌)和三种正常细胞系(结肠上皮、乳腺上皮和成纤维细胞)中维生素K依赖性蛋白的合成情况。我们的结果如下:1)在所研究的所有恶性和正常细胞系中均存在维生素K依赖性羧化酶活性。2)恶性和正常细胞系均合成一族维生素K依赖性蛋白。这些蛋白的微粒体前体的表观分子量为74、62和34 kDa,所有恶性和正常细胞系都有,而分子量更高和更低的前体似乎仅由部分而非全部肿瘤细胞系合成。3)结肠癌和乳腺癌合成的74 kDa前体被明确鉴定为蛋白S的前体。