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A role for novel adipose tissue‐secreted factors in obesity‐related carcinogenesis
Author(s) -
Cabia B.,
Andrade S.,
Carreira M. C.,
Casanueva F. F.,
Crujeiras A. B.
Publication year - 2016
Publication title -
obesity reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.845
H-Index - 162
eISSN - 1467-789X
pISSN - 1467-7881
DOI - 10.1111/obr.12377
Subject(s) - adipokine , chemerin , adiponectin , resistin , adipose tissue , medicine , leptin , carcinogenesis , endocrinology , apelin , obesity , cancer , insulin resistance , receptor
Summary Obesity, a pandemic disease, is caused by an excessive accumulation of fat that can have detrimental effects on health. Adipose tissue plays a very important endocrine role, secreting different molecules that affect body physiology. In obesity, this function is altered, leading to a dysfunctional production of several factors, known as adipocytokines. This process has been linked to various comorbidities associated with obesity, such as carcinogenesis. In fact, several classical adipocytokines with increased levels in obesity have been demonstrated to exert a pro‐carcinogenic role, including leptin, TNF‐α, IL‐6 and resistin, whereas others like adiponectin, with decreased levels in obesity, might have an anti‐carcinogenic function. In this expanding field, new proteomic techniques and approaches have allowed the identification of novel adipocytokines, a number of which exhibit an altered production in obesity and type 2 diabetes and thus are related to adiposity. Many of these novel adipocytokines have also been identified in various tumour types, such as that of the breast, liver or endometrium, thereby increasing the list of potential contributors to carcinogenesis. This review is focused on the regulation of these novel adipocytokines by obesity, including apelin, endotrophin, FABP4, lipocalin 2, omentin‐1, visfatin, chemerin, ANGPTL2 or osteopontin, emphasizing its involvement in tumorigenesis.