4.7 Article

CD44 Mediates Oral Squamous Cell Carcinoma-Promoting Activity of MRE11 via AKT Signaling

期刊

JOURNAL OF PERSONALIZED MEDICINE
卷 12, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/jpm12050841

关键词

oral squamous cell carcinoma; CD44; cancer sternness; tumorsphere; metastasis; MRE11

资金

  1. Ministry of Science and Technology [MOST1102314-B-037-058, MOST110-2314-B-037-129, MOST110-2314-B-037-084]
  2. Kaohsiung Medical University Hospital [KMUH108-8R42, KMUH109-9R42, KMUH110-0R43]
  3. Kaohsiung Medical University [KMU-DK108005, KMU-DK109001, KMU-DK(A)110001, KMU-DK(A)111005]
  4. NSYSU-KMU Joint Research Project in Taiwan [NSYSUKMU108-P034, NSYSUKMU109-I004]

向作者/读者索取更多资源

Oral cancer is a highly prevalent malignancy worldwide, and cancer stemness may hinder its management. This study reveals that MRE11 enhances the malignancy of OSCC cells through the induction of CD44.
Oral cancer is one of the highest-incidence malignancies worldwide, with the occurrence of oral squamous cell carcinoma (OSCC) being the most frequently diagnosed form. A barrier for oral cancer management may arise from tumor cells that possess properties of cancer stemness, which has been recognized as a crucial factor in tumor recurrence and metastasis. As such, understanding the molecular mechanisms underlying these tumor cells may provide insights for improving cancer treatment. MRE11 is the core protein of the RAD50/MRE11/NBS1 complex with a primary role in DNA damage repair, and it has been diversely associated with tumor development including OSCC. In this study, we aimed to investigate the engagement of CD44, a cancer stemness marker functioning in the control of cell growth and motility, in OSCC malignancy under the influence of MRE11. We found that overexpression of MRE11 enhanced CD44 expression and tumorsphere formation in OSCC cells, whereas knockdown of MRE11 reduced these phenomena. In addition, the MRE11-promoted tumorsphere formation or cell migration ability was compromised in OSCC cells carrying siRNA that targets CD44, as was the MRE11-promoted AKT phosphorylation. These were further supported by analyzing clinical samples, where higher CD44 expression was associated with lymph node metastasis. Additionally, a positive correlation between the expression of MRE11 and CD44, or that of CD44 and phosphorylated AKT, was observed in OSCC tumor tissues. Finally, the expression of CD44 was found to be higher in the metastatic lung nodules from mice receiving tail vein-injection with MRE11-overexpressing OSCC cells compared with control mice, and a positive correlation between CD44 and phosphorylated AKT was also observed in these metastatic lung nodules. Altogether, our current study revealed a previously unidentified mechanism linking CD44 and AKT in MRE11-promoted OSCC malignancy, which may shed light to the development of novel therapeutic strategies in consideration of this new pathway in OSCC.

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