TY - JOUR
T1 - Tgf-ß alterations in oral squamous cell carcinoma
AU - Candia, Jorge
AU - Somarriva, Carolina
AU - Fonseca, Diego
AU - Parada, Fernando
AU - Briceño, Jorge
AU - Fernández, Alejandra
N1 - Publisher Copyright:
© 2016 - Official publication of the Facultad de Odontología, Universidad de Concepción.
PY - 2016
Y1 - 2016
N2 - The transforming growth factor beta (TGF-ß) is a cytokine that plays crucial roles in the regulation of angiogenesis, immune response, proliferation, migration and apoptosis of cells. In addition, it can inhibit cell progression and stimulate apoptosis in early stages of cancer. TGF-ß is a multifunctional homodimeric protein secreted by various cell lines, which have three different isoforms: TGF-ß1, TGF-ß2 and TGF-ß3. In normal conditions, TGF-ß1 activates some tumor suppressor cell signaling pathways that inhibit proliferation and are involved in cell migration, differentiation and apoptosis. However, in more advanced stages of cancer, when TGF-ß1 is altered, it acts as a promoter of tumorigenesis and may cause: 1) increased TGF-ß1, 2) overexpression of TGF-ß1 receptors (TßR), 3) TßR mutations, and 4) downregulation of TGF-beta receptor. In oral squamous cell carcinoma, the path is altered especially at the level of transmembrane receptors, with the TßR-II and TßR-III subtypes being the most affected. However, there is little information on the prognostic role it plays in the various types of cancers. It is important to study the signaling pathways of TGF-ß in order to develop techniques that may help detect their alterations and restore their normal operation. The objective of this review is to describe the alterations of TGF-ß in oral squamous cell carcinoma.
AB - The transforming growth factor beta (TGF-ß) is a cytokine that plays crucial roles in the regulation of angiogenesis, immune response, proliferation, migration and apoptosis of cells. In addition, it can inhibit cell progression and stimulate apoptosis in early stages of cancer. TGF-ß is a multifunctional homodimeric protein secreted by various cell lines, which have three different isoforms: TGF-ß1, TGF-ß2 and TGF-ß3. In normal conditions, TGF-ß1 activates some tumor suppressor cell signaling pathways that inhibit proliferation and are involved in cell migration, differentiation and apoptosis. However, in more advanced stages of cancer, when TGF-ß1 is altered, it acts as a promoter of tumorigenesis and may cause: 1) increased TGF-ß1, 2) overexpression of TGF-ß1 receptors (TßR), 3) TßR mutations, and 4) downregulation of TGF-beta receptor. In oral squamous cell carcinoma, the path is altered especially at the level of transmembrane receptors, with the TßR-II and TßR-III subtypes being the most affected. However, there is little information on the prognostic role it plays in the various types of cancers. It is important to study the signaling pathways of TGF-ß in order to develop techniques that may help detect their alterations and restore their normal operation. The objective of this review is to describe the alterations of TGF-ß in oral squamous cell carcinoma.
KW - Oral cancer
KW - Smad4 protein
KW - Squamous cell carcinoma
KW - Transforming growth factor beta1
UR - http://www.scopus.com/inward/record.url?scp=84986608412&partnerID=8YFLogxK
U2 - 10.17126/joralres.2016.045
DO - 10.17126/joralres.2016.045
M3 - Review article
AN - SCOPUS:84986608412
SN - 0719-2479
VL - 5
SP - 207
EP - 214
JO - Journal of Oral Research
JF - Journal of Oral Research
IS - 5
ER -