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1.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 31(4): 1233-1236, 2023 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-37551504

RESUMO

Multiple myeloma (MM) is a malignant proliferative disease of plasma cells. Bone marrow mesenchymal stem cells (MSC) play an important role in the progression of MM. Compared with normal donor derived MSC (ND-MSC), MM patients derived MSC (MM-MSC) exhibit abnormalities in genes, signaling pathways, protein expression levels and cytokines secreted by themselves. Moreover, the exosomes of MM-MSC can interact with the bone marrow microenvironment. The above reasons can lead to MM cell proliferation, chemoresistance, impaired osteogenic differentiation of MM-MSC, and affect the immunomodulatory capacity of MM patients. In order to further understand the pathogenesis and related influencing factors of MM, this paper reviews the latest research progress of MM-MSC.


Assuntos
Células-Tronco Mesenquimais , Mieloma Múltiplo , Humanos , Mieloma Múltiplo/patologia , Osteogênese , Diferenciação Celular , Medula Óssea/metabolismo , Células da Medula Óssea/metabolismo , Microambiente Tumoral
2.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 30(4): 1286-1290, 2022 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-35981400

RESUMO

Myelodysplastic syndrome (MDS) are a heterogeneous group of hematological malignancies. Currently, in addition to demethylated chemotherapy and hematopoietic stem cell transplantation, MDS patient-derived mesenchymal stem cells (MDS-MSC) play an important role in understanding the pathogenesis of MDS and related therapeutic targets. For example, abnormal expression of DICER1 gene, abnormalities of PI3K/AKT and Wnt/ß-catenin signaling pathways provide new therapeutic targets for MDS. In addition, MDS-MSC is also affected by abnormal microenvironment of the body, such as inflammatory factor S100A9, as well as hypercoagulation and iron overload. In this review, genes, signaling pathways, cytokines, hematopoietic microenvironment, and the effect of therapeutic drugs for MDS-MSC were briefly summarized.


Assuntos
Neoplasias Hematológicas , Células-Tronco Mesenquimais , Síndromes Mielodisplásicas , Citocinas/metabolismo , RNA Helicases DEAD-box/metabolismo , Neoplasias Hematológicas/metabolismo , Humanos , Síndromes Mielodisplásicas/genética , Fosfatidilinositol 3-Quinases/metabolismo , Ribonuclease III/metabolismo , Microambiente Tumoral
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