Douglas Alexsander Alves
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Douglas Alexsander Alves has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Bruno de Carvalho Dornelas
Postgraduate Program in Health Sciences, Medical School, Federal University of Uberlândia (FAMED-UFU), Uberlândia 38405-320, Minas Gerais, Brazil
2 shared publications - Lara Vecchi
Laboratory of Nanobiotechnology, Federal University of Uberlandia, Uberlandia 38400-902, MG, Brazil
2 shared publications - Luiz Ricardo Goulart
Institute of Biotechnology, Federal University of Uberlândia, Uberlândia 38405-320, MG, Brazil
2 shared publications - Sara Teixeira Soares Mota
Laboratory of Nanobiotechnology, Institute of Genetics and Biochemistry, Federal University of Uberlândia, Campus Umuarama, Bloco 2E, Sala 248, 38400-902 Uberlândia, Brazil
2 shared publications - Stephania Martins Bezerra
Department of Pathological Anatomy, Fundação Antônio Prudente, A.C. Camargo Cancer Center, Rua Prof. Antônio Prudente, São Paulo, Brazil
2 shared publications - Thaise Gonçalves Araújo
Universidade Federal de Uberlândia, Brasil; Universidade Federal de Uberlândia, Brasil
2 shared publications
Latest Publications
- 1 October 2020
- Published by Elsevier in The International Journal of Biochemistry & Cell Biology
- Vol. 127, 105838
Annexin A1 promotes the nuclear localization of the epidermal growth factor receptor in castration-resistant prostate cancer
- 1 October 2020
- Published by Elsevier in The International Journal of Biochemistry & Cell Biology
- Vol. 127, 105838
Annexin A1 promotes the nuclear localization of the epidermal growth factor receptor in castration-resistant prostate cancer
- Open Access
- 12 June 2019
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 20 (12) , 2852
New Insights into the Role of Polybromo-1 in Prostate Cancer
The human protein Polybromo-1 (PBMR1/BAF180) is a component of the SWI/SNF chromatin-remodeling complex that has been reported to be deregulated in tumors. However, its role in prostate cancer (PCa) is largely unknown. In this study, we described the PBRM1 transcriptional levels and the protein expression/localization in tissues of PCa patients and in prostatic cell lines. Increased PBRM1 mRNA levels were found in PCa samples, when compared to benign disease, and were correlated with higher Gleason score. We also verified that only the nuclear localization of PBRM1 protein is correlated with a more aggressive disease and high Prostate-Specific Antigen (PSA) levels in tissue microarrays. Intriguing expression patterns of mRNA and protein were identified in the cell lines. Although PBRM1 protein was restricted to the nuclei, in tumor cell lines in non-neoplastic cells, it was also present in vesicular-like structures that were dispersed within the cytoplasm. We knocked-down PBRM1 in the castration-resistant PCa (CRPC) cell line PC-3 and we verified that PBRM1 promotes the expression of several markers of aggressiveness, including EpCAM, TGF-β, and N-Cadherin. Therefore, our data supported the hypothesis that PBRM1 displays a pivotal role in the promotion and maintenance of the malignant behavior of PCa, especially in CRPC.
- 12 June 2019
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 20 (12) , 2852
Open AccessNew Insights into the Role of Polybromo-1 in Prostate Cancer
The human protein Polybromo-1 (PBMR1/BAF180) is a component of the SWI/SNF chromatin-remodeling complex that has been reported to be deregulated in tumors. However, its role in prostate cancer (PCa) is largely unknown. In this study, we described the PBRM1 transcriptional levels and the protein expression/localization in tissues of PCa patients and in prostatic cell lines. Increased PBRM1 mRNA levels were found in PCa samples, when compared to benign disease, and were correlated with higher Gleason score. We also verified that only the nuclear localization of PBRM1 protein is correlated with a more aggressive disease and high Prostate-Specific Antigen (PSA) levels in tissue microarrays. Intriguing expression patterns of mRNA and protein were identified in the cell lines. Although PBRM1 protein was restricted to the nuclei, in tumor cell lines in non-neoplastic cells, it was also present in vesicular-like structures that were dispersed within the cytoplasm. We knocked-down PBRM1 in the castration-resistant PCa (CRPC) cell line PC-3 and we verified that PBRM1 promotes the expression of several markers of aggressiveness, including EpCAM, TGF-β, and N-Cadherin. Therefore, our data supported the hypothesis that PBRM1 displays a pivotal role in the promotion and maintenance of the malignant behavior of PCa, especially in CRPC.