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通过各种抑制剂研究干扰素处理的巨噬细胞的细胞毒性活性。

Cytotoxic activity of interferon-treated macrophages studied by various inhibitors.

作者信息

Schultz R M, Pavlidis N A, Stylos W A, Chirigos M A

出版信息

Cancer Treat Rep. 1978 Nov;62(11):1889-92.

PMID:728906
Abstract

The ability of interferon-treated macrophages to kill or inhibit the growth of tumor cells is markedly influenced by the local environment. The macrophage cytotoxic effector system is regulated by serum and other environmental factors that suppress tumor killing. Prostaglandins E1 and E2, but not F2alpha reversibly inhibited the tumoricidal state of interferon-treated macrophages. Hydrocortisone was similarly active at suppressing macrophage function. Such nonimmunologically derived factors could prevent the final triggering step for macrophage-mediated tumor killing in the local environment of the tumor and may be important in the pathogenesis of progressive tumor growth.

摘要

经干扰素处理的巨噬细胞杀伤或抑制肿瘤细胞生长的能力受到局部环境的显著影响。巨噬细胞细胞毒性效应系统受血清和其他抑制肿瘤杀伤的环境因素调节。前列腺素E1和E2而非F2α可可逆地抑制经干扰素处理的巨噬细胞的杀肿瘤状态。氢化可的松在抑制巨噬细胞功能方面同样具有活性。这类非免疫源性因素可能会阻止肿瘤局部环境中巨噬细胞介导的肿瘤杀伤的最终触发步骤,并且在肿瘤进行性生长的发病机制中可能很重要。

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