TP53 Gene Alterations and P53 Protein Accumulation in Human Esophageal Cancer in Khartoum State, Sudan.

Journal Title: IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) - Year 2018, Vol 17, Issue 11

Abstract

TP53 gene alterations were screened in 50 formalin fixed paraffin embedded (FFPE) human esophageal cancer (EC) specimens comprising 43 squamous cell carcinoma (SCC) and 7 adenocarcinoma (AC) using immunohistochemistry (IHC) and conventional PCR followed by DNA sequencing to detect p53 accumulation and mutation, respectively, in Khartoum state, Sudan. TP53 gene mutations were detected in 20 (40%) of the 50 EC cases investigated. Five out of 13 (38.5%) of SCC cases that stained positive for p53 protein, showed TP53 mutations, only one (14.3%) of seven AC samples was positive for p53 protein without associated mutation and 4/7 (57.1%) showed TP53 mutations only. Immunohistochemical stain was positive in 14/50 (28%) of EC samples; 13 (92.9%) of them were SSC cases and one (7.1%) AC. Five out of forty three (11.6%) of SSC and none of AC cases showed both immunohistochemical positive stain and mutation of TP53 gene while 8/43 (18.6%) of SSC and 1/7 (14.3%) of AC samples showed immunohistochemical positive stain but no TP53 gene mutation were present. Finally 15/50 (30%) of EC, 11 (73.3%) were SSC and 4 (26.7 %) AC showed immunohistochemical negative stain and positive TP53 gene mutations. Immunohistochemical patterns of p53 were not related significantly to mutational analysis results in the cases examined. Mutation analysis is recommended to be done on the entire length of the gene using fresh tissue to complete the whole picture in future studies.

Authors and Affiliations

Rihab M. Elfaki, Mohammed S. AbdelAziz, Hisham N. Eltayb, Munsoor M. Munsoor, Ahmed A. Gameel

Keywords

Related Articles

Gorlin Goltz Syndrome – Case Series and Review of Literature.

The Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome (NBCCS), is an infrequent multisystemic disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable exp...

Echocardiographic Pattern of Rheumatic Heart Disease In Makurdi Nigeria.

Background: Rheumatic heart disease (RHD) remains a major cause of acquired heart disease in children and adults in developing countries. Sub-Saharan Africa has been described as the major hotspot for acute rheumatic fev...

Profile of Adverse Drug Reaction Related Hospitalization ina Tertiary Care Teaching Hospital

Adverse drug reactions are a major problem worldwide and are one among the leading causes of morbidity and mortality. They are an important cause of hospitalization or prolongation of hospital stay. This study was conduc...

Prediction of Cancerous Cell by Cluster Based Biomedical CT Image and Analysis

Medical and health arena is advanced in recent years with the technological influence especially using image processing techniques and algorithms. Biomedical Image processing resolves many cons of manual disease recognit...

Prevalence Of Adverse Events Related To Blood Transfusion At Tertiary Care Center Of Central India.

Background: Although blood transfusion is an essential part of medical treatment but it is also associated with significant clinical risks due to blood components’ allogenic origin. In recent testing facilities have lowe...

Download PDF file
  • EP ID EP416496
  • DOI 10.9790/0853-1711086267.
  • Views 47
  • Downloads 0

How To Cite

Rihab M. Elfaki, Mohammed S. AbdelAziz, Hisham N. Eltayb, Munsoor M. Munsoor, Ahmed A. Gameel (2018). TP53 Gene Alterations and P53 Protein Accumulation in Human Esophageal Cancer in Khartoum State, Sudan.. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS), 17(11), 62-67. https://europub.co.uk/articles/-A-416496