Department of Pathology, K S Hegde Medical Academy, Nitte (Deemed to be University), Deralakatte, Mangalore, Karnataka, India.
Department of Biochemistry, JSS Medical College, JSS Academy of Higher Education and Research, Mysuru, Karnataka, India.
J Cancer Res Ther. 2024 Jul 1;20(5):1440-1445. doi: 10.4103/jcrt.jcrt_1226_22. Epub 2024 Jan 22.
Oesophageal malignancies (OC) are the sixth most common cause of cancer-related mortality worldwide. Traditional risk factors for OC include smoking, alcohol consumption, and poorly controlled acid reflux; however, the trends in the last decade have pointed out the potential carcinogenic roles of infectious agents, especially Human Papillomavirus (HPV), in the development of OC. The prevalence of HPV infection in OC varies greatly worldwide, mainly due to the inconsistencies of the detection assays employed. This study attempted to establish the association between high-risk HPV and oesophageal malignancies by detecting the transcriptionally active HPV mRNA.
In this cross-sectional study, 30 malignant oesophageal samples were subjected to real-time PCR to detect high-risk HPV-16 and 18 by targeting transcriptionally active E6/E7 genes. The positive samples were further subjected to viral load assessment.
Histopathological analysis of the patients showed that a moderately differentiated squamous cell carcinoma was seen in 56.2% of the cases. Of the 30 samples, 4 (13.3%) showed positive for HPV-16 E6/E7, and none showed positive for HPV-18 E6/E7. The viral load of HPV-16 E6/E7 in the positive samples was lesser than the copies present in the well-established cell line, SiHa.
The role of HPV in the etiopathogenesis of oesophageal malignancies is unclear. Based on this study and the supporting data presented, it can be said that the association of high-risk HPV infection in oesophageal cancers does exist, but whether it is clinically and etiologically significant is the question that needs to be answered. Multicenter studies from different geographical locations, employing multiple molecular methods with a larger sample size, could aid in a better understanding of the etiopathogenesis of HPV in OC.
食管恶性肿瘤(OC)是全球第六大常见的癌症相关死亡原因。OC 的传统危险因素包括吸烟、饮酒和胃酸反流控制不佳;然而,过去十年的趋势指出了感染因子(尤其是人乳头瘤病毒(HPV))在 OC 发展中的潜在致癌作用。HPV 感染在 OC 中的流行程度在全球范围内差异很大,主要是由于所使用的检测方法不一致。本研究试图通过检测转录活跃的 HPV mRNA 来建立高危 HPV 与食管恶性肿瘤之间的关联。
在这项横断面研究中,对 30 份恶性食管样本进行实时 PCR 检测,以针对转录活跃的 E6/E7 基因检测高危 HPV-16 和 18。阳性样本进一步进行病毒载量评估。
患者的组织病理学分析显示,56.2%的病例为中分化鳞状细胞癌。在 30 个样本中,有 4 个(13.3%)显示 HPV-16 E6/E7 阳性,而没有一个显示 HPV-18 E6/E7 阳性。阳性样本中 HPV-16 E6/E7 的病毒载量低于已建立的 SiHa 细胞系中的拷贝数。
HPV 在食管恶性肿瘤发病机制中的作用尚不清楚。基于本研究和提出的支持数据,可以说高危 HPV 感染与食管癌症之间存在关联,但它在临床上和病因学上是否具有重要意义是需要回答的问题。来自不同地理位置的多中心研究,采用多种分子方法和更大的样本量,可以帮助更好地理解 HPV 在 OC 中的发病机制。