Oncotarget

Research Papers:

Assessment of circularized E7 RNA, GLUT1, and PD-L1 in anal squamous cell carcinoma

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Oncotarget. 2019; 10:5958-5969. https://doi.org/10.18632/oncotarget.27234

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Bahir H. Chamseddin, Eunice E. Lee, Jiwoong Kim, Xiaowei Zhan, Rong Yang, Kathleen M. Murphy, Cheryl Lewis, Gregory A. Hosler, Suntrea T. Hammer and Richard C. Wang _

Abstract

Bahir H. Chamseddin1, Eunice E. Lee1, Jiwoong Kim2, Xiaowei Zhan2, Rong Yang1, Kathleen M. Murphy3, Cheryl Lewis4, Gregory A. Hosler1,3,*, Suntrea T. Hammer5,* and Richard C. Wang1,3,*

1 Department of Dermatology, UT Southwestern Medical Center, Dallas, 75390, TX, USA

2 Department of Clinical Science, UT Southwestern Medical Center, Dallas, 75390, TX, USA

3 ProPath Dermatopathology, Dallas, 75247, TX, USA

4 Harold C. Simmons Center, UT Southwestern Medical Center, Dallas, 75390, TX, USA

5 Department of Pathology, UT Southwestern Medical Center, Dallas, 75390, TX, USA

* These authors contributed equally to this work

Correspondence to:

Richard C. Wang,email: richard.wang@utsouthwestern.edu

Keywords: anal squamous cell carcinoma; circular RNA; GLUT1; human papillomavirus; PD-L1

Received: August 02, 2019     Accepted: September 23, 2019     Published: October 15, 2019

ABSTRACT

Anal squamous cell carcinoma (ASCC) is a rare, potentially fatal malignancy primarily caused by high-risk human papillomaviruses (HPV). The prognostic implication of programmed death-ligand 1 (PD-L1) expression remains controversial, and glucose transporter 1 (GLUT1) expression has never been examined in ASCC. Covalently closed circular RNAs have recently been shown to be widespread in cancers and are proposed to be biomarkers. We discovered HPV16 expresses a circular E7 RNA (circE7) which has not been assessed as a potential biomarker. A retrospective, translational case series at UT Southwestern was conducted to analyze PD-L1, GLUT1, HPV-ISH, and HPV circE7 in relation to the clinical features and overall survival of patients with ASCC. Twenty-two (22) subjects were included in the study. Improved overall survival was predicted by basaloid histology (p = 0.013), PD-L1 expression (p = 0.08), and HPV-ISH positivity (p < 0.001), but not GLUT1 expression. High levels of circE7 by quantitative RT-PCR predicted improved overall survival in ASCC (p = 0.023) and analysis of The Cancer Genome Atlas sequencing from HPV-positive head and neck cancer and cervical cancer suggested high circE7 marked improved survival in 875 subjects (p = 0.074). While our study suggests that circE7 levels correlate with improved survival in ASCC, larger, prospective studies are necessary to confirm the potential role of circE7 as a biomarker.



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