癌症
医学
乳腺癌
表观遗传学
风险因素
人口
血管生成
癌细胞
前瞻性队列研究
生物信息学
癌症研究
肿瘤科
遗传学
免疫学
内科学
基因
生物
环境卫生
作者
David Gunnell,Mona Okasha,George Davey Smith,SE Oliver,Jat Sandhu,Jeffrey M P Holly
标识
DOI:10.1093/oxfordjournals.epirev.a000809
摘要
Associations between height and cancer risk have been
reported in a number of prospective studies (1, 2). Taller
individuals appear to be at increased risk. Furthermore, ecologic
analyses indicate that geographic patterns of cancer
incidence and mortality are associated with variations in
population height (3-5). The most consistent associations
have been found in relation to breast cancer (6-8), although
associations have also been reported for many other cancer
sites. Therefore, common mechanisms may underlie these
associations, but their precise nature remains unclear.
Models of cancer pathogenesis suggest that cancer arises
as a result of DNA damage at a number of specific loci
important in the regulation of the cell cycle or DNA repair
(9, 10). While specific oncogenes, tumor suppresser genes,
and cancer susceptibility genes have been identified, it has
become increasingly apparent that epigenetic pathways also
underlie the development of some malignancies. Several
mechanisms may be common to many different cancers. For
example, angiogenesis (the formation of new blood vessels)
is an absolute requirement for the growth of all solid tumors
(11). Similarly, apoptosis is a mechanism for eliminating
damaged or dangerous cells from the body, and thus it provides
a natural defense against cancer. The most potent cell
survival factor controlling apoptosis is insulin-like growth
factor I (IGF-I). Raised levels of IGF-I and reduced levels of
its main binding protein, insulin-like growth factor (IGF)-
binding protein 3, may diminish this defense against a range
of cancers. In support of this notion, recent prospective
research has demonstrated that raised levels of IGF-I are
associated with increased risks of prostate (12-14), breast
(15), and colorectal (16, 17) cancers.
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