Expression and Correlation of HER2/P53/VEGF in Marjolin’s Ulcer

Author:

Xia Chen1,Chu Zhigang2,Wu Yiqi3

Affiliation:

1. Department of Pathology, Wuhan Third Hospital & Tongren Hospital of Wuhan University , Wuhan , China

2. Burns Department, Wuhan Third Hospital & Tongren Hospital of Wuhan University , Wuhan , China

3. Department of Urology, Renmin Hosptial of Wuhan University , Wuhan 430060 , China

Abstract

Abstract Marjolin’s ulcer is described as malignant lesions developed in the injured skin, which can cause several kinds of malignancies. Our results showed that no HER2 but p53 was detected in Majorlin’s ulcer samples. Meanwhile, by statistical analysis, we found that the positive rate of p53 in Majorlin’s ulcer samples was associated with the pathological type of ulcer canceration and degree of tumor differentiation. The positive expression rate of vascular endothelial growth factor (VEGF) was 62.5% in poorly differentiated squamous cell carcinoma (SCC), 39.4% in moderately differentiated SCC, and 66.7% in well-differentiated SCC, respectively. Furthermore, some cases of Majorlin’s ulcer with positive P53 were negative for VEGF, while some cases with positive VEGF were negative for P53. Image superposition showed that VEGF expression was absent or minimal in p53-positive cases. However, P53 was not expressed or rarely expressed in VEGF-positive cases. Our results of this study will suggest that P53 can be used as the mark of Marjolin’s ulcer differentiation, and there may be some interaction between P53 and VEGF in Marjolin’s ulcer. The regulation of microenvironment in the oncogenesis, progression, and differentiation of Marjolin’s ulcer is complex and needs further study.

Funder

Wuhan Health and Family Planning Commission Project

Publisher

Oxford University Press (OUP)

Subject

Rehabilitation,Emergency Medicine,Surgery

Reference31 articles.

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2. Activating HER2 mutations as emerging targets in multiple solid cancers;Connell,2017

3. Microenvironment-mediated mechanisms of resistance to HER2 inhibitors differ between HER2+ breast cancer subtypes;Watson,2018

4. The role of HER2 as a therapeutic biomarker in gynaecological malignancy: potential for use beyond uterine serous carcinoma;Talia,2023

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