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分泌人肿瘤坏死因子/恶病质素的肿瘤可在小鼠中诱发恶病质。

Tumors secreting human TNF/cachectin induce cachexia in mice.

作者信息

Oliff A, Defeo-Jones D, Boyer M, Martinez D, Kiefer D, Vuocolo G, Wolfe A, Socher S H

出版信息

Cell. 1987 Aug 14;50(4):555-63. doi: 10.1016/0092-8674(87)90028-6.

Abstract

Anorexia and weight loss are serious complications that adversely effect the prognosis of cancer patients. It has been suggested that TNF/cachectin may cause cachexia. To determine if TNF/cachectin can induce progressive weight loss in tumor-bearing animals, a clone of the human TNF/cachectin gene was isolated and inserted into a mammalian expression vector. This construct was transfected into CHO cells, and a cell line (CHO/TNF-20) that secretes TNF/cachectin was isolated. A cell line (CHO/CMV-Neo) that contains the same expression vector without the TNF/cachectin gene was also isolated. Nude mice injected intraperitoneally with CHO/TNF-20 cells died more quickly than mice injected with CHO/CMV-Neo cells. Eighty-seven percent of mice inoculated intramuscularly with CHO/TNF-20 cells developed severe cachexia and weight loss. All mice bearing CHO/CMV-Neo tumors maintained or increased their body weight. We conclude that mice bearing tumors that secrete TNF/cachectin develop progressive wasting and die more quickly than mice bearing control tumors.

摘要

厌食和体重减轻是严重的并发症,会对癌症患者的预后产生不利影响。有人提出肿瘤坏死因子/恶病质素可能导致恶病质。为了确定肿瘤坏死因子/恶病质素是否能在荷瘤动物中引起进行性体重减轻,分离了人肿瘤坏死因子/恶病质素基因的一个克隆,并将其插入到一个哺乳动物表达载体中。将该构建体转染到CHO细胞中,分离出分泌肿瘤坏死因子/恶病质素的细胞系(CHO/TNF-20)。还分离出了一个含有相同表达载体但不含肿瘤坏死因子/恶病质素基因的细胞系(CHO/CMV-Neo)。腹腔注射CHO/TNF-20细胞的裸鼠比注射CHO/CMV-Neo细胞的小鼠死亡更快。肌肉注射CHO/TNF-20细胞的小鼠中,87%出现严重恶病质和体重减轻。所有携带CHO/CMV-Neo肿瘤的小鼠体重维持不变或增加。我们得出结论,与携带对照肿瘤的小鼠相比,携带分泌肿瘤坏死因子/恶病质素肿瘤的小鼠会出现进行性消瘦且死亡更快。

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