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The Association of Molecular Biomarkers in the Diagnosis of Cervical Pre-Cancer and Cancer and Risk Factors in Senegalese

机译:分子生物标志物在塞内加尔宫颈前癌症和癌症和危险因素的诊断中的关联

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Background: Cervical intraepithelial neoplasia (CIN) grading is subjective and affected by substantial rates of discordance among pathologists. Although recent studies have suggested that p16INK4a may be a useful surrogate biomarker of cervical neoplasia, Ki-67 and human papillomavirus testing have also been shown to be useful in detecting neoplasia. The purpose of this study was to determine the expression of p16INK4a and Ki-67 in cervical neoplasia and its correlations with cofactors. Methods: The study involved 69 patients with and without cervical neoplasia who underwent colposcopic directed biopsy. On each patient, two samples were taken; the first was used for immunohistochemistry and the second for molecular testing, using HPV16and18 genotyping Real-Time PCR Kit. Results: The study revealed the expression level of p16INK4a and Ki-67 in a descending order, from invasive squamous cell carcinoma (SCC), CIN2/3, CIN1 and non-dysplastic lesions. Correlations showed an association between the staining of p16NK4a and Ki-67 with the increase of age (OR: 1.79 (95%IC: 0.49 – 6.55), p = 0.037) and marital status (OR: 0.17 (95%IC: 0.04 – 0.68), p = 0.003). We found that the expressions of p16INK4a and Ki-67 were significantly different between invasive SCC vs non-dysplasia (OR: 44.57 (95%IC: 4.91 – 403.91), p 0.0001). The study showed significant correlation between HPV 16and18 infection with p16 INK4a and Ki-67 expression (OR: 0.13 (95%IC: 0.03 – 0.52), p 0.0001). Strong expression of p16INK4a and Ki-67 were observed in invasive squamous cell carcinoma, moderate staining was found in CIN2/3, weak staining in CIN1 and normal histology. Conclusion: Our findings indicate that p16INK4a and Ki-67 expressions associated strongly with cervical pathology. Therefore, p16/Ki-67 could be considered as a suitable biomarker for cervical cancer screening, particularly in HPV-based screening programs.
机译:背景:宫颈上皮内肿瘤(CIN)分级是主观的,受病理学家之间的重要性的主观性的。尽管最近的研究表明p16ink4a可以是宫颈瘤形成的有用的替代生物标志物,但ki-67和人乳头瘤病毒检测也已被证明可用于检测肿瘤。本研究的目的是确定宫颈瘤形成中p16ink4a和ki-67的表达及其与辅因子的相关性。方法:该研究涉及69例患有宫颈瘤形成的患者,患有阴道镜诊断的活检。在每位患者身上,拍摄了两个样品;首批用于免疫组织化学和第二种用于分子检测,使用HPV16和18基因分型实时PCR试剂盒。结果:该研究揭示了P16ink4a和Ki-67以降序,来自侵入性鳞状细胞癌(SCC),CIN2 / 3,CIN1和非发育性病变的表达水平。相关性与年龄的增加(或:1.79(95%IC:0.49-6.55),P = 0.037)和婚姻状况(或:0.17(95%IC:0.04 - 0.68),p = 0.003)。我们发现,P16ink4a和Ki-67的表达在侵入性SCC与非发育不良(或:44.57(95%IC:4.91-403.91),P <0.0001)之间具有显着差异。该研究表明,HPV 16Ad18感染与P16 Ink4a和Ki-67表达(或:0.13(95%Ic:0.03-0.52),P <0.0001)之间的关联相关。在侵袭性鳞状细胞癌中观察到p16ink4a和ki-67的强烈表达,中等染色在CIN2 / 3中发现,CIN1弱染色和正常组织学。结论:我们的研究结果表明,宫颈病理学强烈相关的p16ink4a和ki-67表达。因此,P16 / KI-67可以被认为是用于宫颈癌筛选的合适生物标志物,特别是在基于HPV的筛查计划中。

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