切断癌症与肥胖之间的必经之路

【字体: 时间:2015年11月11日 来源:生物通

编辑推荐:

  近年来关于肥胖与癌症的研究都集中在预防癌症的行为干预方面了,但是对于全球将近7亿的肥胖成人来说,除了减肥植物,更有效的措施是减轻他们患病风险,美国临床肿瘤学会,世界癌症研究基金会等组织指出,肥胖相关的癌症就会是下个十年,癌症研究领域最为紧迫的问题。

   ——肥胖人群患癌风险确实比较高,而且一旦被确诊会出现更差的预后效果,并产生化疗耐药性,那么问题来了,这是为什么呢?

生物通报道:肥胖症的流行速度令人震惊,在世界范围内,估计有22亿成人属于超重或肥胖的范畴,其中许多都出现了代谢综合征的症状:血压升高和高水平血糖和胆固醇,还有循环胰岛素水平增加,炎性细胞因子增多等等。这些代谢和免疫的变化虽然本身已经成为了一种问题,但这并不是肥胖人口所面临的唯一的健康问题——肥胖会增加多种慢性疾病的患病风险和恶化风险,其中包括多种类型的癌症。今年,肥胖已经超越吸烟,成为了美国癌症死亡的首要因素。

问题一:肥胖和癌症存在什么关联?

近年来关于肥胖与癌症的研究都集中在预防癌症的行为干预方面了,但是对于全球将近7亿的肥胖成人来说,除了减肥植物,更有效的措施是减轻他们患病风险,美国临床肿瘤学会,世界癌症研究基金会等组织指出,肥胖相关的癌症就会是下个十年,癌症研究领域最为紧迫的问题。

(有十种类型的癌症与超重或肥胖有关,不仅肥胖会增加癌症的患病风险,而且这也是存活率降低,预后差,更快转移的一个诱导因素)

(胰岛素抵抗:许多肥胖患者都会出现胰岛素抵抗,而追踪激素的增多,也会促进癌症的发生,以及化疗耐药性的发生)

(细胞信号:介导相邻细胞之间的信号通路被干扰,这也会促进肿瘤发生和发展)

(活性脂肪:在肥胖患者体内肿瘤微环境中的脂肪细胞更为活跃,能分泌多种促癌激素和细胞因子)

(炎症:与肥胖有关的代谢变化也会刺激巨噬细胞生成过量的促炎症化合物,从而促进癌症发展,或通过诱发DNA损伤,抑制细胞凋亡,刺激细胞迁移和侵袭,来诱发癌症)

(肠道微生物组: 肥胖会导致肠道细菌多样性减少,损伤肠道屏障功能,令譬如脂多糖 (LPS)之类的细菌化合物渗漏到肠道之外。这又会进一步增加炎症,并促进癌症发展。)

 

下篇:

 下个十年,癌症研究最为紧迫是肥胖问题

原文文献:

Breaking the Cancer-Obesity Link(来自http://www.the-scientist.com/)

K. Subbaramaiah et al., “Increased levels of COX-2 and prostaglandin E2 contribute to elevated aromatase expression in inflamed breast tissue of obese women,” Cancer Discov, 2:356-65, 2012.
P.G. Morris et al., “Inflammation and increased aromatase expression occur in the breast tissue of obese women with breast cancer,” Cancer Prev Res, 4:1021-29, 2011.
S. Chen et al., “Obesity or overweight is associated with worse pathological response to neoadjuvant chemotherapy among Chinese women with breast cancer,” PLOS ONE, 7:e41380, 2012.
B. Guiu et al., “Visceral fat area is an independent predictive biomarker of outcome after first-line bevacizumab-based treatment in metastatic colorectal cancer,” Gut, 59:341-47, 2010.
J. Chen et al., “Insulin caused drug resistance to oxaliplatin in colon cancer cell line HT29,” J Gastrointest Oncol, 2:27-33, 2011
R.E. De Angel et al., “Stearoyl gemcitabine nanoparticles overcome obesity-induced resistance to gemcitabine in a mouse model of breast cancer,” Cancer Biol Ther, 14:357-64, 2013.
Y. Naguib et al., “Solid lipid nanoparticle formulations of docetaxel prepared with high-melting point triglycerides: In vitro and in vivo evaluation,” Mol Pharm, 11:1239-49, 2014.
L.M. Nogueira et al., “Calorie restriction and rapamycin inhibit MMTV-Wnt-1 mammary tumor growth in a mouse model of postmenopausal obesity,” Endocr Relat Cancer, 19:57-68, 2012.
H. Liu et al., “Metformin and the mTOR inhibitor everolimus (RAD001) sensitize breast cancer cells to the cytotoxic effect of chemotherapeutic drugs in vitro,” Anticancer Res, 32:1627-37, 2012.
H. Liu et al., “The mTOR inhibitor RAD001 sensitizes tumor cells to the cytotoxic effect of carboplatin in breast cancer in vitro,” Anticancer Res, 31:2713-22, 2011.
C.J. Fabian et al., “Favorable modulation of benign breast tissue and serum risk biomarkers is associated with >10% weight loss in postmenopausal women,” Breast Cancer Res Treat, 142:119-32, 2013.
R.E. De Angel et al., “The enhancing effects of obesity on mammary tumor growth and Akt/mTOR pathway activation persist after weight loss and are reversed by Rad001,” Mol Carcinog, 52:446-58, 2013.
S.D. Hursting et al., “The obesity-cancer link: Lessons learned from a fatless mouse,” Cancer Res, 67:2391-93, 2007.
K. Aung et al., “Risk of developing diabetes and cardiovascular disease in metabolically unhealthy normal-wight and metabolically healthy obese individuals,” J Clin Endocrinol, 99:462-68, 2014.
P. Pajunen et al., “Metabolically healthy and unhealthy obesity phenotypes in the general population,” BMC Public Health, 11:754, 2011.

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