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Author
- Aguilera, Paula1
- Badenas, Celia1
- Cabré, Eduard1
- Fabra, Àngels1
- Ferreres, Josep R1
- Jia, Jinjing1
- Lai, Baochang1
- Lei, Ting1
- Li, Changji1
- Liu-Smith, Feng1
- Luo, Suju1
- Malvehy, Josep1
- Marcoval, Joaquim1
- Mateo, Francesca1
- Palomero, Luís1
- Piulats, Josep M1
- Puig, Susana1
- Puig-Butille, Joan Anton1
- Pujana, Miquel A1
- Shao, Yongping1
- Tell-Martí, Gemma1
- Vinyals, Antònia1
- Wang, Nanping1
- Wang, Qiongyu1
- Wang, Xin1
Keyword
- extracellular signal-regulated kinase2
- MEK2
- 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide1
- 5-fluorouracil1
- 5-Fu1
- amphiregulin1
- AREG1
- cell cycle gene homology region1
- CHR1
- cSCC1
- cutaneous squamous cell carcinoma1
- EMT1
- epithelial-mesenchymal transition1
- FBS1
- fetal bovine serum1
- m1
- MAPK1
- MMP1
- MTT1
- PI1
- TCGA1
- The Cancer Genome Atlas Network1
- YAP1
Melanoma
2 Results
- Original Article Melanocytes/MelanomaOpen Archive
AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy
Journal of Investigative DermatologyVol. 137Issue 6p1297–1310Published online: February 7, 2017- Joan Anton Puig-Butille
- Antònia Vinyals
- Josep R. Ferreres
- Paula Aguilera
- Eduard Cabré
- Gemma Tell-Martí
- and others
Cited in Scopus: 33The cell cycle-related genes AURKA and FOXM1 are overexpressed in melanoma. We show here that AURKA overexpression is associated with poor prognosis in three independent cohorts of melanoma patients and correlates with the presence of genomic amplification of AURKA locus and BRAFV600E mutation. AURKA overexpression may also be driven by increased promoter activation through elements such as ETS and FOXM1 found within the 5′ proximal promoter region. Activated MAPK/ERK signaling pathway mediates robust AURKA promoter activation, thereby knockdown of BRAFV600E and ERK inhibition results in reduced AURKA transcription and expression. - Original Article Tumor BiologyOpen Archive
Yes-Associated Protein Contributes to the Development of Human Cutaneous Squamous Cell Carcinoma via Activation of RAS
Journal of Investigative DermatologyVol. 136Issue 6p1267–1277Published online: February 20, 2016- Jinjing Jia
- Changji Li
- Suju Luo
- Feng Liu-Smith
- Jiao Yang
- Xin Wang
- and others
Cited in Scopus: 33Cutaneous squamous cell carcinoma (cSCC) is one of the most common skin malignant tumors with an increasing incidence. Studies have shown that Yes-associated protein (YAP) participates in the development of a variety of tumors as an oncogene, but to our knowledge its role in cSCC has not been reported. In this study, we used immunohistochemistry to show that YAP expression was elevated in cSCC samples of different stages versus in normal skin and that it was well correlated with the progression of the disease.