Breast cancer protection by genomic imprinting in close kin families

被引:3
作者
Denic, Srdjan [1 ]
Agarwal, Mukesh M. [2 ]
机构
[1] United Arab Emirates Univ, Dept Med, Coll Med & Hlth Sci, POB 17666, Abu Dhabi, U Arab Emirates
[2] Calif Univ Sci & Med, Dept Pathol, 217 E Club Ctr Dr, San Bernardino, CA 92408 USA
关键词
Public health; Mate selection; Epigenetics; Homozygosis; Heterosis; Arabs; Pakistan; ACUTE LYMPHOBLASTIC-LEUKEMIA; GLUTATHIONE-S-TRANSFERASES; UMBILICAL-CORD BLOOD; LOW-BIRTH-WEIGHT; GESTATIONAL-AGE; BRCA2; MUTATIONS; SAUDI-ARABIA; FLUCTUATING ASYMMETRY; PLACENTAL EXPRESSION; OVARIAN-CANCER;
D O I
10.1186/s12881-017-0498-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human inbreeding generally reduces breast cancer risk (BCR). When the parents are biologically related, their infants have a lower birth weight due to smaller body organs. The undersized breasts, because of fewer mammary stem cells, have a lower likelihood of malignant conversion. Fetal growth is regulated by genomically imprinted genes which are in conflict; they promote growth when derived from the father and suppress growth when derived from the mother. The kinship theory explicates that the intensity of conflict between these genes affects growth and therefore the size of the newborn. In descendants of closely related parents, this gene clash is less resulting in a smaller infant. In this review, we elucidate the different mechanisms by which human inbreeding affects BCR, and why this risk is dissimilar in different inbred populations.
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页数:8
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