1.Cancerous Inhibitor of Protein Phosphatase 2A as aMolecular Marker for Aggressiveness and Survival in OralSquamous Cell Carcinoma
Rajab ALZAHRANI ; Amani A. ALREHAILI ; Amal F. GHARIB ; Farah ANJUM ; Khadiga A. ISMAIL ; Wael H. ELSAWY
Journal of Cancer Prevention 2020;25(1):21-26
Cancerous inhibitor of protein phosphatase 2A (CIP2A) has been identified as one of the most commonly altered proteins in humancancers. It blocks the tumor-suppressive action of protein phosphatase 2A (PP2A) complex and enhances malignancy. Thirty-fivepatients with squamous cell carcinoma of the oral cavity underwent surgical resection of the tumor. CIP2A was assessed by quantitativereal-time PCR in the resected tumor tissues and in their adjacent normal tissues. CIP2A was found to be overexpressed inall oral squamous cell carcinoma (OSCC) specimens in comparison to their surrounding normal tissue. CIP2A overexpression wasstatistically correlated with poor prognostic feature of the tumor. Thus, a high expression level of CIP2A was associated with shortersurvival. In conclusion, CIP2A is upregulated in OSCC, and its overexpression is correlated with aggressiveness of the tumor andpoor outcome and survival. It may serve as a prognostic marker of OSCC.
2.Sequence Analysis of Hypothetical Proteins from Helicobacter pylori 26695 to Identify Potential Virulence Factors.
Ahmad Abu Turab NAQVI ; Farah ANJUM ; Faez Iqbal KHAN ; Asimul ISLAM ; Faizan AHMAD ; Md Imtaiyaz HASSAN
Genomics & Informatics 2016;14(3):125-135
Helicobacter pylori is a Gram-negative bacteria that is responsible for gastritis in human. Its spiral flagellated body helps in locomotion and colonization in the host environment. It is capable of living in the highly acidic environment of the stomach with the help of acid adaptive genes. The genome of H. pylori 26695 strain contains 1,555 coding genes that encode 1,445 proteins. Out of these, 340 proteins are characterized as hypothetical proteins (HP). This study involves extensive analysis of the HPs using an established pipeline which comprises various bioinformatics tools and databases to find out probable functions of the HPs and identification of virulence factors. After extensive analysis of all the 340 HPs, we found that 104 HPs are showing characteristic similarities with the proteins with known functions. Thus, on the basis of such similarities, we assigned probable functions to 104 HPs with high confidence and precision. All the predicted HPs contain representative members of diverse functional classes of proteins such as enzymes, transporters, binding proteins, regulatory proteins, proteins involved in cellular processes and other proteins with miscellaneous functions. Therefore, we classified 104 HPs into aforementioned functional groups. During the virulence factors analysis of the HPs, we found 11 HPs are showing significant virulence. The identification of virulence proteins with the help their predicted functions may pave the way for drug target estimation and development of effective drug to counter the activity of that protein.
Carrier Proteins
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Clinical Coding
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Colon
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Computational Biology
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Drug Discovery
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Gastritis
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Genome
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Gram-Negative Bacteria
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Helicobacter pylori*
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Helicobacter*
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Humans
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Locomotion
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Sequence Analysis*
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Stomach
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Virulence Factors*
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Virulence*