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抗阻运动抑制两种癌鼠模型的肿瘤生长。

Resistance Exercise Counteracts Tumor Growth in Two Carcinoma Rodent Models.

机构信息

Department of Physical Education, State University of Londrina, Londrina, PR, BRAZIL.

Department of General Pathology, State University of Londrina, Londrina, PR, BRAZIL.

出版信息

Med Sci Sports Exerc. 2019 Oct;51(10):2003-2011. doi: 10.1249/MSS.0000000000002009.

Abstract

PURPOSE

Although resistance exercise (RE) is now recognized as an adjuvant in cancer treatment because of its capacity to prevent muscle wasting, weakness, and cachexia, it is unknown whether RE can mitigate tumor development. Two solid adenocarcinoma models (Walker-256 and Ehrlich) were used to investigate the effects of RE on tumor cell proliferation, growth, and aggressiveness parameters in tumor-bearing animals' life span.

METHODS

Walker-256 tumor-bearing rats and Ehrlich tumor-bearing mice were subjected to RE, which consisted of climbing a ladder apparatus with loads tied to their tails. After 4 wk, animals were euthanized, and tumors were excised and assessed for tumor microenvironment evaluation such as cell proliferation and apoptosis determination, collagen deposit, and presence of malignant tumor morphology.

RESULTS

Our data demonstrate that RE mitigated tumor growth and favored tumor end points such as lower Scarff-Bloom-Richardson histological grade tumor, denoting slow cell aberrant form and division, decreased tumor cell proliferation (evaluated by nucleus marked with antigen ki-67), and lower viable tumor area in both types of tumors studied. In addition, RE stimulated tumor microvessel density in Walker-256 tumor-bearing rats, but there was no change in their life span.

CONCLUSION

RE may mitigate tumor growth and tumor malignancy parameters such as lower histopathological grade, assuming less nuclear pleomorphism and mitotic cells, smaller viable tumor area, and decreased tumor cell proliferation in both adenocarcinomas. In addition, RE induced tumor vascularization.

摘要

目的

尽管阻力运动(RE)现在因其预防肌肉消耗、虚弱和恶病质的能力而被认为是癌症治疗的辅助手段,但尚不清楚 RE 是否可以减轻肿瘤的发展。使用两种实体腺癌模型(Walker-256 和 Ehrlich)来研究 RE 对肿瘤-bearing 动物寿命期间肿瘤细胞增殖、生长和侵袭性参数的影响。

方法

Walker-256 肿瘤-bearing 大鼠和 Ehrlich 肿瘤-bearing 小鼠接受 RE,即尾巴上绑有负载物的攀爬梯设备。4 周后,处死动物,切除肿瘤并评估肿瘤微环境,如细胞增殖和凋亡测定、胶原沉积以及恶性肿瘤形态的存在。

结果

我们的数据表明,RE 减轻了肿瘤的生长,并有利于肿瘤终点,如较低的 Scarff-Bloom-Richardson 组织学分级肿瘤,提示细胞异常形态和分裂较慢、肿瘤细胞增殖减少(用抗原 ki-67 标记的细胞核评估),以及两种研究肿瘤的存活肿瘤面积减小。此外,RE 刺激了 Walker-256 肿瘤-bearing 大鼠的肿瘤微血管密度,但它们的寿命没有变化。

结论

RE 可能减轻肿瘤生长和肿瘤恶性参数,如较低的组织病理学分级、假设较少的核多形性和有丝分裂细胞、较小的存活肿瘤面积和降低肿瘤细胞增殖在两种腺癌中。此外,RE 诱导了肿瘤血管生成。

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