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Cheng, G.Z., Zhang, W.Z., Sun, M., Wang, Q., Coppola, D., Mansour, M., Xu, L.M., Costanzo, C., Cheng, J.Q. and Wang, L.H. (2008) Twist is transcriptionally induced by activation of STAT3 and mediates STAT3 oncogenic function. The Journal of Biological Chemistry, 283, 14665- 14673. doi:10.1074/jbc.M707429200

has been cited by the following article:

• TITLE: Embryoprotein TWIST distribution in breast cancer cells MDA-MB-231 treated with 5-Fluorouracil and malnutrition

  AUTHORS: Jesica Escobar-Cabrera, Angelina Rodríguez-Torres, Laura Berumen-Segura, Guadalupe García Alcocer

  KEYWORDS: TWIST; Breast Cancer; 5-Fu; 5-Fluorouracil; NEAA; Nonessential Amino Acid

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.4 No.12, December 9, 2011

  ABSTRACT: TWIST is a transcription factor that belongs to the family of helix-loop-helix proteins involved in metastasis with essential role regulating cell movement during early development, as well as in the tumor progression and metastasis of many cancers including breast cancer. It will be interesting to study the relation among cancer chemotherapy, malnutrition and the transcription factors like TWIST in order to explore the risk to metastasis. We used breast cancer line MDA-MB-231. Cell cultures were treated with 5-Fluorouracil (5-Fu), as well as changes in serum and nonessentials amino acid (NEAA), to explore the cell viability and the cellular distribution of TWIST by immunocytochemistry. Our results indicate that cell viability decreased significantly with 5-Fu treatment whereas no changes were observed in malnutrition treatment. On the other hand, TWIST protein significantly increased its distribution in cytoplasm of treated groups with malnutrition as well as in those treated with 5-Fu compared with the control. These results suggest that TWIST translocation was modified by the treatments and further studies are necessary to suggest that TWIST could be a tag protein to avoid metastasis.