ALCAM-EGFR interaction regulates myelomagenesis

Author:

Luo Hongmei12,Zhang Dan12,Wang Fangfang12,Wang Qiang3ORCID,Wu Yu1,Gou Maling2,Hu Yiguo2ORCID,Zhang Wenyan4,Huang Jingcao12ORCID,Gong Yuping1,Pan Ling1,Li Tianshu3,Zhao Pan1,Zhang Danfeng1,Qu Ying12,Liu Zhigang1,Jiang Tao1,Dai Yang1,Guo Tingting1,Zhu Jiang5,Ye Lingqun3ORCID,Zhang Li1,Liu Weiping4,Yi Qing3ORCID,Zheng Yuhuan12

Affiliation:

1. Department of Hematology, West China Hospital,

2. State Key Laboratory of Biotherapy and Cancer Center, Sichuan University, Chengdu, China;

3. Center for Translational Research in Hematological Malignancies, Cancer Center, Houston Methodist Hospital, Houston, TX;

4. Department of Pathology; and

5. Department of Oncology, West China Hospital, Sichuan University, Chengdu, China

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Hematology

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