Yamamura K, Kibbey M C, Jun S H, Kleinman H K
Laboratory of Developmental Biology, National Institute of Dental Research, NIH, Bethesda, MD 20892.
Semin Cancer Biol. 1993 Aug;4(4):259-65.
Basement membrane has a variety of effects on tumor cells and promotes malignant behavior. Tumor cell growth is enhanced both in vitro and in vivo in mice in the presence of basement membrane. This has led to the ability to grow various tumors including human biopsy specimens in nude mice. Furthermore, low cell numbers can be used when coinjected with Matrigel, a basement membrane extract. The basement membrane glycoprotein laminin is important in promoting invasive behavior and the level of a 32/67 kDa laminin receptor has been shown to correlate with malignancy. A sequence of five amino acids, tyrosine-isoleucine-glycine-serine-arginine (YIGSR) has been shown to recognize this receptor and to reduce experimental metastases (tail vein injection resulting in colonization of the lung) and subcutaneous tumor growth. This peptide is active in both models either when coinjected or when daily intraperitoneal injections are given after tumor growth has initiated. YIGSR does not effect cell arrest but does inhibit angiogenesis which is necessary for tumor growth. YIGSR also appears to have an additional antitumor effect via its interaction with a specific receptor. YIGSR-adherent cells established after 30 successive selections on YIGSR-coated dishes in vitro formed more lung colonies after intravenous injection and larger tumors after subcutaneous injection than the parent B16F10 melanoma cells. The YIGSR-non-adherent cells formed fewer lung colonies and smaller subcutaneous tumors. These data demonstrate the importance of laminin-tumor cell interactions in malignancies and suggest that a short sequence from laminin has multiple effects in reducing tumor growth and spread.(ABSTRACT TRUNCATED AT 250 WORDS)
基底膜对肿瘤细胞有多种影响,并促进其恶性行为。在基底膜存在的情况下,小鼠体内外的肿瘤细胞生长均得到增强。这使得包括人类活检标本在内的各种肿瘤能够在裸鼠体内生长。此外,与基底膜提取物基质胶共同注射时,可以使用少量细胞进行实验。基底膜糖蛋白层粘连蛋白在促进侵袭行为方面很重要,并且已证明32/67 kDa层粘连蛋白受体的水平与恶性程度相关。已证明由酪氨酸-异亮氨酸-甘氨酸-丝氨酸-精氨酸(YIGSR)组成的五肽序列可识别该受体,并减少实验性转移(尾静脉注射导致肺部定植)和皮下肿瘤生长。无论是共同注射还是在肿瘤生长开始后每日腹腔注射,该肽在两种模型中均具有活性。YIGSR不会影响细胞停滞,但会抑制肿瘤生长所必需的血管生成。YIGSR似乎还通过与特定受体的相互作用产生额外的抗肿瘤作用。在体外YIGSR包被的培养皿上连续选择30次后建立的YIGSR黏附细胞,静脉注射后形成更多的肺集落,皮下注射后形成比亲本B16F10黑色素瘤细胞更大的肿瘤。YIGSR非黏附细胞形成的肺集落较少,皮下肿瘤较小。这些数据证明了层粘连蛋白与肿瘤细胞相互作用在恶性肿瘤中的重要性,并表明层粘连蛋白的一个短序列在减少肿瘤生长和扩散方面具有多种作用。(摘要截短至250字)