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ALCAM-EGFR interaction regulates myelomagenesis

Multiple myeloma, a plasma cell malignancy in the bone marrow, remains largely incurable with currently available therapeutics. In this study, we discovered that the activated leukocyte cell adhesion molecule (ALCAM) interacted with epidermal growth factor receptor (EGFR), and regulated myelomagenes...

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Detalles Bibliográficos
Autores principales: Luo, Hongmei, Zhang, Dan, Wang, Fangfang, Wang, Qiang, Wu, Yu, Gou, Maling, Hu, Yiguo, Zhang, Wenyan, Huang, Jingcao, Gong, Yuping, Pan, Ling, Li, Tianshu, Zhao, Pan, Zhang, Danfeng, Qu, Ying, Liu, Zhigang, Jiang, Tao, Dai, Yang, Guo, Tingting, Zhu, Jiang, Ye, Lingqun, Zhang, Li, Liu, Weiping, Yi, Qing, Zheng, Yuhuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152994/
https://www.ncbi.nlm.nih.gov/pubmed/34592762
http://dx.doi.org/10.1182/bloodadvances.2021004695
Descripción
Sumario:Multiple myeloma, a plasma cell malignancy in the bone marrow, remains largely incurable with currently available therapeutics. In this study, we discovered that the activated leukocyte cell adhesion molecule (ALCAM) interacted with epidermal growth factor receptor (EGFR), and regulated myelomagenesis. ALCAM was a negative regulator of myeloma clonogenicity. ALCAM expression was positively correlated with patients’ survival. ALCAM-knockdown myeloma cells displayed enhanced colony formation in the presence of bone marrow stromal cells (BMSCs). BMSCs supported myeloma colony formation by secreted epidermal growth factor (EGF), which bound with its receptor (EGFR) on myeloma cells and activated Mek/Erk cell signaling, PI3K/Akt cell signaling, and hedgehog pathway. ALCAM could also bind with EGFR, block EGF from binding to EGFR, and abolish EGFR-initiated cell signaling. Hence, our study identifies ALCAM as a novel negative regulator of myeloma pathogenesis.