Department of Otorhinolaryngology Head and Neck Surgery, University Medical Centre Mannheim, 68167 Mannheim, Germany.
Oncol Rep. 2013 Jun;29(6):2325-31. doi: 10.3892/or.2013.2380. Epub 2013 Apr 3.
Stromal cell-derived factor-1α (SDF-1α), also known as CXCL12, has variable effects on a plurality of cells. CXCR4 has been identified as its corresponding receptor. The SDF-1-CXCR4 axis is postulated to be a crucial key pathway in the interaction between (cancer) stem cells and their surrounding supportive cells in the cancer stem cell niche. We evaluated the expression of CD44 as a cancer stem cell marker and of CXCR4 in human HNSCC tissue samples. Afterwards, we monitored the concentration of SDF-1 in peripheral blood samples of HNSCC patients and healthy donors. We showed that CD44 and CXCR4 are expressed in human HNSCC tissues. Markedly, CD44 showed a high expression in HNSCC cells bordering cancer stromal cells. CXCR4 was mainly expressed in HNSCC tumor nests, but not in the surrounding stromal cells. No significant difference was noted between the SDF-1 concentration in the peripheral blood of HNSCC patients compared to healthy donors. We showed that CD44, as a stem cell marker in HNSCC, is located mainly at the borderline of HNSCC tumor nests with the surrounding cells. In addition, we demonstrated that CXCR4 as the corresponding receptor to SDF-1 is highly expressed in HNSCC tumor nests, but not in the tumor stroma. We collected evidence that SDF-1-CXCR4 interaction may be a crucial pathway in cell trafficking in the cancer stem cell niche of HNSCC, while SDF-1 was not detected in the peripheral blood of HNSCC patients. The SDF-1-CXCR4 axis may play an important role in the cancer stem cell theory of HNSCC. As SDF-1α also exhibits a multitude of functional effects on HNSCC cells, such as migration and polarization, it may be possible that the SDF-1-CXCR4 axis is also involved in the pathophysiology of the progression, recurrence and metastasis of malignant disease. Understanding these interactions may help to gain further insight into these mechanisms and as such help to discover new strategies of therapy.
基质细胞衍生因子-1α(SDF-1α),也称为 CXCL12,对多种细胞具有不同的影响。CXCR4 已被鉴定为其相应的受体。SDF-1-CXCR4 轴被认为是癌症干细胞及其在癌症干细胞生态位中周围支持细胞相互作用的关键关键途径。我们评估了 CD44 作为癌症干细胞标志物和 CXCR4 在人类头颈部鳞状细胞癌(HNSCC)组织样本中的表达。之后,我们监测了 HNSCC 患者和健康供体外周血样本中 SDF-1 的浓度。我们表明 CD44 和 CXCR4 均在人类 HNSCC 组织中表达。值得注意的是,CD44 在与癌症基质细胞相邻的 HNSCC 细胞中表达较高。CXCR4 主要在 HNSCC 肿瘤巢中表达,但不在周围基质细胞中表达。HNSCC 患者与健康供体外周血中的 SDF-1 浓度无显著差异。我们表明,CD44 作为 HNSCC 中的干细胞标志物,主要位于 HNSCC 肿瘤巢与周围细胞的边界处。此外,我们证明 SDF-1 的相应受体 CXCR4 在 HNSCC 肿瘤巢中高度表达,但不在肿瘤基质中表达。我们收集的证据表明,SDF-1-CXCR4 相互作用可能是 HNSCC 癌症干细胞生态位中细胞迁移的关键途径,而在 HNSCC 患者的外周血中未检测到 SDF-1。SDF-1-CXCR4 轴可能在 HNSCC 的癌症干细胞理论中起重要作用。由于 SDF-1α 对 HNSCC 细胞也具有多种功能作用,例如迁移和极化,因此 SDF-1-CXCR4 轴可能也参与恶性疾病进展、复发和转移的病理生理学。了解这些相互作用可能有助于进一步深入了解这些机制,并因此有助于发现新的治疗策略。