Erythropoietin-mediated activation of JAK-STAT signaling contributes to cellular invasion in head and neck squamous cell carcinoma

被引:146
作者
Lai, SY
Childs, EE
Xi, SC
Coppelli, FM
Gooding, WE
Wells, A
Ferris, RL
Grandis, JR
机构
[1] Univ Pittsburgh, Inst Canc, Inst Eye & Ear, Dept Otolaryngol Head & Neck Surg, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Inst Canc, Dept Immunol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Inst Canc, Dept Pathol, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Inst Canc, Dept Pharmacol, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Inst Canc, Sch Med, Pittsburgh, PA 15213 USA
[6] Univ Pittsburgh, Inst Canc, Biostat Facil, Pittsburgh, PA 15213 USA
关键词
erythropoietin; erythropoietin receptor; head and neck cancer; invasion; HNSCC; JAK-STAT;
D O I
10.1038/sj.onc.1208635
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Originally characterized as a growth factor for erythrocytes, erythropoietin (EPO) is used to treat anemia and fatigue in cancer patients receiving radiation therapy and chemotherapy. EPO and the EPO receptor (EPOR) are expressed in nonhematopoietic cells and cancers. However, the role of EPO and EPOR within nonhematopoietic cancer cells remains incompletely understood. Although a recent clinical trial demonstrated worse tumor control and survival in head and neck cancer patients treated with EPO, the role of EPO and EPOR in head and neck squamous cell carcinoma (HNSCC) has not been examined. In the present study, we demonstrate the previously unrecognized EPO-mediated invasion by HNSCC cells through the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling pathway. Furthermore, we confirmed the expression of EPO and EPOR in a panel of human HNSCC cell lines and tissue specimens. Pharmacological doses of EPO also had a limited proliferation effect in these cell lines. These results de. ne a novel role for EPO in mediating tumor cell invasion. Increased levels of EPO and EPOR in lymph node metastases as compared to primary tumors from HNSCC patients further support the role of EPO/EPOR in HNSCC disease progression and metastasis.
引用
收藏
页码:4442 / 4449
页数:8
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