Saleh Tareq, Himsawi Nisreen, Al Rousan Amani, Alhesa Ahmad, El-Sadoni Mohammed, Khawaldeh Suzan, Shahin Nisreen Abu, Ghalioun Ala' Abu, Shawish Bayan, Friehat Kholoud, Alotaibi Moureq R, Abu Al Karsaneh Ola, Abu-Humaidan Anas, Khasawneh Rame, Khasawneh Ashraf I, Al Shboul Sofian
Department of Pharmacology and Public Health, Faculty of Medicine, The Hashemite University, Zarqa 13133, Jordan.
Department of Microbiology, Pathology and Forensic Medicine, Faculty of Medicine, The Hashemite University, Zarqa 13133, Jordan.
Curr Issues Mol Biol. 2024 Dec 2;46(12):13696-13712. doi: 10.3390/cimb46120818.
Oncogene-induced senescence (OIS) is a form of cellular senescence triggered by oncogenic signaling and, potentially, by infection with oncogenic viruses. The role of senescence, along with its associated secretory phenotype, in the development of cervical cancer remains unclear. Additionally, the expression of the senescence-associated secretory phenotype (SASP) has not yet been explored in cervical premalignant lesions infected by the Human Papilloma Virus (HPV). This study aimed to investigate the expression of OIS and SASP markers in HPV-infected cervical precancerous lesions. We used a set of patient-derived precancerous ( = 32) and noncancerous (chronic cervicitis; = 10) tissue samples to investigate the gene expression of several OIS (, , , and ), and SASP (, , , , and ) biomarkers using qRT-PCR. OIS status was confirmed in precancerous lesions based on Lamin B1 downregulation by immunohistochemical staining. HPV status for all precancerous lesions was tested. Most of the noncancerous samples showed high Lamin B1 expression, however, precancerous lesions exhibited significant Lamin B1 downregulation ( < 0.001). Fifty-five percent of the precancerous samples were positive for HPV infection, with HPV-16 as the dominant genotype. Lamin B1 downregulation coincided with HPV E6 positive expression. and expression was higher in precancerous lesions compared to noncancerous tissue, while LMNB1 was downregulated. The SASP profile of premalignant lesions included elevated and and reduced , , and . this work shall provide an opportunity to further examine the role of OIS and the SASP in the process of malignant cervical transformation.
致癌基因诱导的衰老(OIS)是一种由致癌信号触发的细胞衰老形式,也可能由致癌病毒感染引发。衰老及其相关分泌表型在宫颈癌发展中的作用仍不清楚。此外,在人乳头瘤病毒(HPV)感染的宫颈上皮内瘤变中,衰老相关分泌表型(SASP)的表达尚未得到研究。本研究旨在调查HPV感染的宫颈癌前病变中OIS和SASP标志物的表达。我们使用了一组患者来源的癌前(n = 32)和非癌(慢性宫颈炎;n = 10)组织样本,通过qRT-PCR研究几种OIS(p16、p21、p53和p19ARF)和SASP(IL-6、IL-8、MMP-1、MMP-3和TIMP-1)生物标志物的基因表达。通过免疫组织化学染色基于Lamin B1下调在癌前病变中确认OIS状态。检测了所有癌前病变的HPV状态。大多数非癌样本显示Lamin B1高表达,然而,癌前病变表现出显著的Lamin B1下调(P < 0.001)。55%的癌前样本HPV感染呈阳性,其中HPV-16为主要基因型。Lamin B1下调与HPV E6阳性表达一致。与非癌组织相比,癌前病变中p16和p21表达更高,而LMNB1下调。癌前病变的SASP谱包括IL-6和IL-8升高以及MMP-1、MMP-3和TIMP-1降低。这项工作将为进一步研究OIS和SASP在宫颈恶性转化过程中的作用提供机会。