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mda-7/IL-24:IL-10 基因家族的一个独特成员,可促进针对癌症的毒性。

mda-7/IL-24: a unique member of the IL-10 gene family promoting cancer-targeted toxicity.

机构信息

Department of Human and Molecular Genetics, Virginia Commonwealth University, School of Medicine, Richmond, VA, United States.

出版信息

Cytokine Growth Factor Rev. 2010 Oct;21(5):381-91. doi: 10.1016/j.cytogfr.2010.08.004.

Abstract

Melanoma differentiation associated gene-7/interleukin-24 (mda-7/IL-24) is a unique member of the IL-10 gene family that displays nearly ubiquitous cancer-specific toxicity, with no harmful effects toward normal cells or tissues. mda-7/IL-24 was cloned from human melanoma cells by differentiation induction subtraction hybridization (DISH) and promotes endoplasmic reticulum (ER) stress culminating in apoptosis or toxic autophagy in a broad-spectrum of human cancers, when assayed in cell culture, in vivo in human tumor xenograft mouse models and in a Phase I clinical trial in patients with advanced cancers. This therapeutically active cytokine also induces indirect antitumor activity through inhibition of angiogenesis, stimulation of an antitumor immune response, and sensitization of cancer cells to radiation-, chemotherapy- and antibody-induced killing.

摘要

黑色素瘤分化相关基因-7/白细胞介素-24(mda-7/IL-24)是白细胞介素-10 基因家族的一个独特成员,具有几乎普遍的癌症特异性毒性,对正常细胞或组织没有有害影响。mda-7/IL-24 是通过分化诱导消减杂交(DISH)从人类黑色素瘤细胞中克隆出来的,并在细胞培养、人肿瘤异种移植小鼠模型中以及在晚期癌症患者的 I 期临床试验中,促进内质网(ER)应激,最终导致广泛的人类癌症发生细胞凋亡或有毒自噬。这种治疗活性细胞因子还通过抑制血管生成、刺激抗肿瘤免疫反应以及使癌细胞对辐射、化疗和抗体诱导的杀伤作用敏感来诱导间接抗肿瘤活性。

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The development of MDA-7/IL-24 as a cancer therapeutic.MDA-7/IL-24 的研发作为一种癌症治疗方法。
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