A Comprehensive Pan-Cancer Analysis Identifies CEP55 as a Potential Oncogene and Novel Therapeutic Target

Author:

Zaki Mohamed Samir A.1ORCID,Eldeen Muhammad Alaa2ORCID,Abdulsahib Waleed K.3,Shati Ayed A.4ORCID,Alqahtani Youssef A.4,Al-Qahtani Saleh M.4,Otifi Hassan M.5ORCID,Asiri Ashwag4ORCID,Hassan Hesham M.5,Emam Mohammed Ahmed Hebatallah6,Dawood Samy A.4ORCID,Negm Amr78ORCID,Eid Refaat A.5ORCID

Affiliation:

1. Anatomy Department, College of Medicine, King Khalid University, Abha P.O. Box 62529, Saudi Arabia

2. Cell Biology, Histology & Genetics Division, Biology Department, Faculty of Science, Zagazig University, Zagazig 44519, Egypt

3. Pharmacology and Toxicology Department, College of Pharmacy, Al Farahidi University, Baghdad 00965, Iraq

4. Department of Child Health, College of Medicine, King Khalid University, Abha P.O. Box 62529, Saudi Arabia

5. Pathology Department, College of Medicine, King Khalid University, Abha P.O. Box 62529, Saudi Arabia

6. Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Benha University, Banha 13511, Egypt

7. Department of Chemistry, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia

8. Chemistry Department, Faculty of Science, Mansoura University, Mansoura 35516, Egypt

Abstract

Emerging research findings have shown that a centrosomal protein (CEP55) is a potential oncogene in numerous human malignancies. Nevertheless, no pan-cancer analysis has been conducted to investigate the various aspects and behavior of this oncogene in different human cancerous tissues. Numerous databases were investigated to conduct a detailed analysis of CEP55. Initially, we evaluated the expression of CEP55 in several types of cancers and attempted to find the correlation between that and the stage of the examined malignancies. Then, we conducted a survival analysis to determine the relationship between CEP55 overexpression in malignancies and the patient’s survival. Furthermore, we examined the genetic alteration forms and the methylation status of this oncogene. Additionally, the interference of CEP55 expression with immune cell infiltration, the response to various chemotherapeutic agents, and the putative molecular mechanism of CEP55 in tumorigenesis were investigated. The current study found that CEP55 was upregulated in cancerous tissues versus normal controls where this upregulation was correlated with a poor prognosis in multiple forms of human cancers. Additionally, it influenced the level of different immune cell infiltration and several chemokines levels in the tumor microenvironment in addition to the response to several antitumor drugs. Herein, we provide an in-depth understanding of the oncogenic activities of CEP55, identifying it as a possible predictive marker as well as a specific target for developing anticancer therapies.

Funder

Scientific Research of King Khalid University in Abha, Saudi Arabia

Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia

Publisher

MDPI AG

Subject

Clinical Biochemistry

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