Tinelli Andrea, Vergara Daniele, Martignago Roberta, Leo Giuseppe, Malvasi Antonio, Tinelli Raffaele
Department of Obstetrics and Gynaecology, Vito Fazzi Hospital, Lecce, Italy.
Acta Obstet Gynecol Scand. 2008;87(11):1101-13. doi: 10.1080/00016340802160079.
Endometrial cancer is one of the most common invasive gynecologic malignancies in developed countries and the eighth leading cause of cancer death in women; it typically arises in the sixth or seventh decade of life. The aim of this review was to evaluate possible roles of genetic and socio-biological factors in type I endometrial cancer, largely confined to pre- and perimenopausal women, with a history of estrogen exposure and/or endometrial hyperplasia.
An extensive literature review, from 1990 to 2007 was performed on modifiable risk factors for type I endometrial cancer. Additionally, carcinogenesis mechanisms, biomarker and hormonal and biomolecular approaches to cancer detection, progression and monitoring and socio-biological factors were reviewed.
Several socio-biological and lifestyle characteristics, such as hormone replacement therapy, glycemic index, obesity, alcohol use, antipsychotic medication, melatonin, physical activity and variants in hormone metabolism genes have been identified as risk factors for developing endometrial cancer of type I, the majority of which are associated with excess estrogens causing continued stimulation of the endometrium. There is a genetic link to non-polyposis colorectal cancer syndrome, but association of endometrial cancer risk to other genetic polymorphisms has yielded conflicting results.
Many factors linked to hormonal imbalance, such as obesity, weight change, body size, alcohol, hyper-androgenic states, glycemic index and antidepressant agents, influence the endometrial cancer risk, central to which are endogenous and exogenous estrogen hyperstimulation of the endometrium. Conversely, smoking cigarettes, diet, physical activity and melatonin production seem to reduce the risk of cancer development. Other external factors fit well with the unopposed estrogen theory, but more studies are needed to investigate modifiable and added risk factors for endometrial cancer.
子宫内膜癌是发达国家最常见的侵袭性妇科恶性肿瘤之一,也是女性癌症死亡的第八大主要原因;它通常发生在60或70岁。本综述的目的是评估遗传和社会生物学因素在I型子宫内膜癌中的可能作用,I型子宫内膜癌主要发生在绝经前和围绝经期女性中,这些女性有雌激素暴露和/或子宫内膜增生史。
对1990年至2007年期间I型子宫内膜癌的可改变风险因素进行了广泛的文献综述。此外,还综述了致癌机制、生物标志物以及癌症检测、进展和监测的激素和生物分子方法以及社会生物学因素。
几种社会生物学和生活方式特征,如激素替代疗法、血糖指数、肥胖、饮酒、抗精神病药物、褪黑素、体育活动以及激素代谢基因的变异,已被确定为发生I型子宫内膜癌的风险因素,其中大多数与雌激素过多导致子宫内膜持续受到刺激有关。与非息肉病性结直肠癌综合征存在遗传联系,但子宫内膜癌风险与其他基因多态性的关联结果相互矛盾。
许多与激素失衡相关的因素,如肥胖、体重变化、体型、酒精、高雄激素状态、血糖指数和抗抑郁药,都会影响子宫内膜癌风险,其核心是子宫内膜受到内源性和外源性雌激素的过度刺激。相反,吸烟、饮食、体育活动和褪黑素分泌似乎会降低癌症发生风险。其他外部因素与无对抗雌激素理论相符,但需要更多研究来调查子宫内膜癌的可改变风险因素和新增风险因素。