Literature DB >> 21687952

Multidrug resistance and rhabdomyosarcoma (Review).

Consolación Melguizo1, Jose Prados, Ana R Rama, Raúl Ortiz, Pablo J Álvarez, Juan E Fernández, Antonia Aranega.   

Abstract

Classical cytotoxic treatment of rhabdomyosarcoma (RMS) is often accompanied by significant morbidity and poor response. This cytotoxic therapy may induce a multidrug resistance (MDR) phenotype in RMS which is associated with decreased effectiveness of chemotherapy. The majority of MDR molecules belong to a family of ABC (ATP binding cassette) transporters. Studies of drug resistance in RMS suggest that there are various mechanisms acting simultaneously, which might explain the low percentage of long-term survival in this malignancy. Moreover, although cells exposed to cytotoxic agents increase expression of muscle differentiation markers indicating myogenic differentiation, multidrug resistance may be a major obstacle in differentiation therapy for RMS. This review briefly discusses the current knowledge of resistance in RMS and emphasizes the importance of understanding the different aspects of MDR status in these patients.

Entities:  

Mesh:

Year:  2011        PMID: 21687952     DOI: 10.3892/or.2011.1347

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  7 in total

1.  [Not Available].

Authors:  Hassan Bennani; Imad Ziouziou; Jihad El Ghanmi; Tarik Karmouni; Khalid El Khader; Abdellatif Koutani; Ahmed Iben Attya Andaloussi
Journal:  Can Urol Assoc J       Date:  2014-09       Impact factor: 1.862

2.  Combined inhibition of BET bromodomain and mTORC1/2 provides therapeutic advantage for rhabdomyosarcoma by switching cell death mechanism.

Authors:  Ritesh K Srivastava; Purushotham Guroji; Lin Jin; M Shahid Mukhtar; Mohammad Athar
Journal:  Mol Carcinog       Date:  2022-04-26       Impact factor: 5.139

3.  Dickkopf-1 Inhibition Reactivates Wnt/β-Catenin Signaling in Rhabdomyosarcoma, Induces Myogenic Markers In Vitro and Impairs Tumor Cell Survival In Vivo.

Authors:  Irina Giralt; Gabriel Gallo-Oller; Natalia Navarro; Patricia Zarzosa; Guillem Pons; Ainara Magdaleno; Miguel F Segura; Constantino Sábado; Raquel Hladun; Diego Arango; José Sánchez de Toledo; Lucas Moreno; Soledad Gallego; Josep Roma
Journal:  Int J Mol Sci       Date:  2021-11-29       Impact factor: 6.208

4.  MEK and MCL-1 sequential inhibition synergize to enhance rhabdomyosarcoma treatment.

Authors:  Clara Alcon; Fernando Martín; Estela Prada; Jaume Mora; Aroa Soriano; Gabriela Guillén; Soledad Gallego; Josep Roma; Josep Samitier; Alberto Villanueva; Joan Montero
Journal:  Cell Death Discov       Date:  2022-04-07

5.  Cell-based small-molecule compound screen identifies fenretinide as potential therapeutic for translocation-positive rhabdomyosarcoma.

Authors:  David Herrero Martín; Aleksandar Boro; Beat W Schäfer
Journal:  PLoS One       Date:  2013-01-25       Impact factor: 3.240

6.  Differential expression of cytochrome P450 enzymes in normal and tumor tissues from childhood rhabdomyosarcoma.

Authors:  Dora Molina-Ortiz; Rafael Camacho-Carranza; José Francisco González-Zamora; Jaime Shalkow-Kalincovstein; Rocío Cárdenas-Cardós; Rosario Ností-Palacios; Araceli Vences-Mejía
Journal:  PLoS One       Date:  2014-04-03       Impact factor: 3.240

7.  Sequential combinations of chemotherapeutic agents with BH3 mimetics to treat rhabdomyosarcoma and avoid resistance.

Authors:  Clara Alcon; Albert Manzano-Muñoz; Estela Prada; Jaume Mora; Aroa Soriano; Gabriela Guillén; Soledad Gallego; Josep Roma; Josep Samitier; Alberto Villanueva; Joan Montero
Journal:  Cell Death Dis       Date:  2020-08-15       Impact factor: 8.469

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.