B-cell lymphoma 2 family members and sarcomas: a promising target in a heterogeneous disease

Author:

Oliveira Rui Caetano1ORCID,Gama João2ORCID,Casanova José3ORCID

Affiliation:

1. Centro de Anatomia Patológica Germano de Sousa, 3000 Coimbra, Portugal. Coimbra Institute for Clinical and Biomedical Research (iCBR), 3000 Coimbra, Portugal. Centre of Investigation on Genetics and Oncobiology (CIMAGO), 3000 Coimbra, Portugal.

2. Pathology Department, Centro Hospitalar e Universitário de Coimbra, 3000 Coimbra, Portugal.

3. Centre of Investigation on Genetics and Oncobiology (CIMAGO), 3000 Coimbra, Portugal. Orthopedic Oncology Department, Centro Hospitalar e Universitário de Coimbra, 3000 Coimbra, Portugal. Faculdade de Medicina da Universidade de Coimbra, 3000 Coimbra, Portugal.

Abstract

Targeting the B-cell lymphoma 2 (Bcl-2) family proteins has been the backbone for hematological malignancies with overall survival improvements. The Bcl-2 family is a major player in apoptosis regulation and, has captured the researcher’s interest in the treatment of solid tumors. Sarcomas are a heterogeneous group of diseases, comprising several entities, with high morbidity and mortality and with few specific therapies available. The treatment for sarcomas is based on platinum regimens, with variable results and poor outcomes, especially in advanced lesions. The high number of different sarcoma entities makes treatment standardization as well as the performance of clinical trials difficult. The use of Bcl-2 family members modifiers has revealed promising results in in vitro and in vivo models and may be a valid option, especially when used in combination with chemotherapy. In this article, a revision of these results and possibilities for the use of Bcl-2 family members inhibitors in sarcomas was performed.

Publisher

Open Exploration Publishing

Subject

Cancer Research,Oncology

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