Pekarek L A, Starr B A, Toledano A Y, Schreiber H
Department of Pathology, University of Chicago, Illinois 60637.
J Exp Med. 1995 Jan 1;181(1):435-40. doi: 10.1084/jem.181.1.435.
As observed for many types of cancers, heritable variants of ultraviolet light-induced tumors often grow more aggressively than the parental tumors. The aggressive growth of some variants is due to the loss of a T cell-recognized tumor-specific antigen; however, other variants retain such antigens. We have analyzed an antigen retention variant and found that the variant tumor cells grow at the same rate as the parental tumor cells in vitro, but grew more rapidly than the parental cells in the T cell-deficient host. The growth of the variant cells was stimulated in vitro by factors released from tumor-induced leukocytes and by several defined growth factors. In addition, the variant cancer cells actually attracted more leukocytes in vitro than the parental cells. Furthermore, elimination of granulocytes in vivo in nude mice by a specific antigranulocyte antibody inhibited the growth of the variant cancer, indicating that this tumor requires granulocytes for rapid growth.
正如在许多类型的癌症中所观察到的那样,紫外线诱导肿瘤的可遗传变体通常比亲代肿瘤生长得更具侵袭性。一些变体的侵袭性生长是由于T细胞识别的肿瘤特异性抗原的丧失;然而,其他变体保留了此类抗原。我们分析了一个抗原保留变体,发现变体肿瘤细胞在体外与亲代肿瘤细胞以相同的速率生长,但在T细胞缺陷宿主中比亲代细胞生长得更快。变体细胞的生长在体外受到肿瘤诱导的白细胞释放的因子以及几种特定生长因子的刺激。此外,变体癌细胞在体外实际上比亲代细胞吸引了更多的白细胞。此外,通过特异性抗粒细胞抗体在体内消除裸鼠中的粒细胞可抑制变体癌症的生长,表明这种肿瘤需要粒细胞才能快速生长。