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α-生育酚、β-胡萝卜素、角黄素和藻类提取物在实验性癌症消退中的肿瘤坏死因子

Tumor necrosis factor in experimental cancer regression with alphatocopherol, beta-carotene, canthaxanthin and algae extract.

作者信息

Shklar G, Schwartz J

机构信息

Department of Oral Medicine and Oral Pathology, Harvard School of Dental Medicine, Boston, MA 02115.

出版信息

Eur J Cancer Clin Oncol. 1988 May;24(5):839-50. doi: 10.1016/0277-5379(88)90192-7.

Abstract

Regression of established hamster buccal pouch carcinoma has recently been demonstrated in association with an induction of tumor necrosis factor alpha in macrophages. Regression of hamster buccal pouch tumors has also been demonstrated following the local injection of alphatocopherol, canthaxanthin and an extract of Spirulina-Dunaliella algae. The current study demonstrates that cancer regression is also accompanied by a significant induction of tumor necrosis factor in macrophages in the tumor area, suggesting a possible mechanism of tumor destruction. One hundred and forty young, male adult hamsters were divided into seven equal groups of 20 animals. Epidermoid carcinomas were induced in right buccal pouches by 14 weeks of painting, three times per week, of a 0.5% solution of 7,12-dimethylbenz(a)anthracene. Groups 1 and 2 were untreated and sham injected controls. Groups 3-7 had injected twice weekly into the right buccal pouches 0.1 ml (1.9 mg/ml of 13-cis-retinoic acid, canthaxanthin, algae extract, beta-carotene and alphatocopherol. After 4 weeks the tumors in groups 3-7 demonstrated varying degrees of regression and the animals were sacrificed and the right buccal pouches excised. Tumor necrosis factor alpha (TNF-alpha) was demonstrated by immunohistochemical techniques. A very significant increase in TNF-alpha positive macrophages was found in the tumor-bearing pouches of animals in groups 5-7. Smaller numbers of TNF-alpha-positive macrophages were found in group 4 pouches and a very slight increase in group 3 pouches.

摘要

最近已证实,既定的仓鼠颊囊癌消退与巨噬细胞中肿瘤坏死因子α的诱导有关。在局部注射α-生育酚、角黄素和螺旋藻-杜氏藻提取物后,仓鼠颊囊肿瘤也出现了消退。当前的研究表明,癌症消退还伴随着肿瘤区域巨噬细胞中肿瘤坏死因子的显著诱导,提示了一种可能的肿瘤破坏机制。140只年轻的成年雄性仓鼠被分成7组,每组20只。通过每周3次、连续14周涂抹0.5%的7,12-二甲基苯并(a)蒽溶液,在右侧颊囊中诱发表皮样癌。第1组和第2组为未治疗的假注射对照组。第3 - 7组每周两次向右侧颊囊注射0.1毫升(1.9毫克/毫升的13-顺式视黄酸、角黄素、藻类提取物、β-胡萝卜素和α-生育酚)。4周后,第3 - 7组的肿瘤出现了不同程度的消退,随后处死动物并切除右侧颊囊。采用免疫组织化学技术检测肿瘤坏死因子α(TNF-α)。在第5 - 7组动物的荷瘤颊囊中,发现TNF-α阳性巨噬细胞显著增加。在第4组颊囊中发现的TNF-α阳性巨噬细胞数量较少,而在第3组颊囊中仅有非常轻微的增加。

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