Description
Made available in DSpace on 2015-03-18T15:55:37Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-01-01Bitstream added on 2015-03-18T16:28:37Z : No. of bitstreams: 1 WOS000340753200001.epub: 900482 bytes, checksum: 9d60d72f74e38a60e8389216b85166a2 (MD5)Bitstream added on 2015-03-18T16:28:37Z : No. of bitstreams: 2 WOS000340753200001.epub: 900482 bytes, checksum: 9d60d72f74e38a60e8389216b85166a2 (MD5) WOS000340753200001.pdf: 1311771 bytes, checksum: 6288cd99b36974bae0c45dcec5c17e6f (MD5)
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
The increased production of reactive oxygen species (ROS) plays a key role in pathogenesis of diabetic complications. ROS are generated by exogenous and endogenous factors such as during hyperglycemia. When ROS production exceeds the detoxification and scavenging capacity of the cell, oxidative stress ensues. Oxidative stress induces DNA damage and when DNA damage exceeds the cellular capacity to repair it, the accumulation of errors can overwhelm the cell resulting in cell death or fixation of genome mutations that can be transmitted to future cell generations. These mutations can lead to and/or play a role in cancer development. This review aims at (i) understanding the types and consequences of DNA damage during hyperglycemic pregnancy; (ii) identifying the biological role of DNA repair during pregnancy, and (iii) proposing clinical interventions to maintain genome integrity. While hyperglycemia can damage the maternal genetic material, the impact of hyperglycemia on fetal cells is still unclear. DNA repair mechanisms may be important to prevent the deleterious effects of hyperglycemia both in mother and in fetus DNA and, as such, prevent the development of diseases in adulthood. Hence, in clinical practice, maternal glycemic control may represent an important point of intervention to prevent the deleterious effects of maternal hyperglycemia to DNA.
Sao Paulo State Univ, Grad Program Gynecol Obstet & Mastol, UNESP, Sao Paulo, Brazil
NIEHS, Mol Carcinogenesis Lab, Durham, NC USA
Univ Sao Paulo, Dept Microbiol, BR-05508 Sao Paulo, Brazil
Univ Sao Paulo, Inst Biomed Sci, Dept Cell & Dev Biol, Sao Paulo, Brazil
Sao Paulo State Univ, Botucatu Med Sch, Dept Obstet & Gynecol, UNESP, BR-18618000 Botucatu, SP, Brazil
Sao Paulo State Univ, Grad Program Gynecol Obstet & Mastol, UNESP, Sao Paulo, Brazil
Sao Paulo State Univ, Botucatu Med Sch, Dept Obstet & Gynecol, UNESP, BR-18618000 Botucatu, SP, Brazil
FAPESP: 11/18240-2
FAPESP: 11/13562-1
FAPESP: 12/23296-0