Literature DB >> 21851221

Expression of cyclin A and bone morphogenetic protein receptors and response to induction therapy in patients with acute leukemias.

Justyna Dzietczenia1, Tomasz Wróbel, Bożena Jaźwiec, Grzegorz Mazur, Aleksandra Butrym, Kazimierz Kuliczkowski.   

Abstract

Bone morphogenetic proteins (BMPs) are multifunctional cytokines that belong to the transforming growth factor β (TGFβ) family. They participate in the regulation of growth, differentiation and apoptosis in a variety of cell types including hematopoietic lineages. To date, the role of BMPs in carcinogenesis has not been well known. Cyclin A is a cell cycle regulatory protein which plays the role of a parameter of cell proliferation in various types of carcinomas including hematological malignancies. The role of BMPRIA, BMPRIB, BMPRI and cyclin A in the pathogenesis of acute leukemias remains unclear. The aim of this study was to evaluate the expression of BMP receptors and cyclin A on blast cells and their possible relationship with clinical outcome. Seventy patients with acute leukemias (28 female and 42 male) and 10 aged-matched healthy controls were studied. All patients were examined before cytostatic treatment. The expression of BMP receptors and cyclin A was detected by flow cytometry. The results show that higher expression of BMPRIA, BMPRIB, BMPRII and cyclin A is related with a higher complete response (CR) rate, higher overall survival (OS) and lower relapse risk. The expressions of BMPRIA, BMPRIB, BMPRII and cyclin A could be useful as prognostic parameters of the proliferation status of acute leukemia cells, but further studies are needed to assess this phenomenon.

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Year:  2011        PMID: 21851221     DOI: 10.3109/10428194.2011.597903

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


  1 in total

1.  Low expression of BMPRIB indicates poor prognosis of breast cancer and is insensitive to taxane-anthracycline chemotherapy.

Authors:  Kun Dai; Fengxia Qin; Huikun Zhang; Xiaoli Liu; Caixia Guo; Ming Zhang; Feng Gu; Li Fu; Yongjie Ma
Journal:  Oncotarget       Date:  2016-01-26
  1 in total

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