Coimbra Eliane Campos, DA Conceição Gomes Leitão Maria, Júnior Marconi Rego Barros, DE Oliveira Talita Helena Araújo, DA Costa Silva Neto Jacinto, DE Freitas Antonio Carlos
Biological Sciences Institute (ICB), University of Pernambuco, Pernambuco, Brazil Laboratory of Molecular Studies and Experimental Therapy (LEMTE), Department of Genetics, Center for Biological Sciences, Federal University of Pernambuco, Pernambuco, Brazil
Laboratory of Molecular Studies and Experimental Therapy (LEMTE), Department of Genetics, Center for Biological Sciences, Federal University of Pernambuco, Pernambuco, Brazil.
Anticancer Res. 2016 Aug;36(8):3939-46.
BACKGROUND/AIM: Host molecules disturbed by human papillomavirus (HPV) oncoproteins have been shown to be potential biomarkers of cervical carcinogenesis and represent an alternative or supplementary aid to cytological testing and HPV detection. The miR-203 and one of its targets, ΔNp63, are known to be host molecules that interact with each other to control the proliferation and differentiation of keratinocytes; both have been found to be dysregulated in many cancers. As the role of p63 and miR-203 in cervical carcinogenesis is not yet well-understood, we have, thus, decided to evaluate the changes of expression of both in cervical carcinogenesis.
This study was carried out by obtaining quantitative polymerase chain reaction (qPCR) data from cervical biopsies.
miR-203 and ΔNp63 displayed a similar expression pattern across cervical tissues and both targets showed statistically significant differences between low-grade squamous intraepithelial lesion (LSIL) x high-grade squamous intraepithelial lesion (HSIL); HSIL x Cancer. Additionally, we did not observe an inverse correlation between ΔNp63 mRNA and miR-203 levels as expected but, rather, a positive correlation between cervical tissues.
Although preliminary, the expression levels of ΔNp63 mRNA and miR-203 seem to be promising for cervical cancer screening. In addition, positive correlation between miR-203 and ΔNp63 expression suggests the possible existence of some indirect pathways. However, further studies are needed to clarify the role of ΔNp63 and miR-203 in cervical carcinogenesis and, thus, determine how they can be applied in new strategies for diagnosis.
背景/目的:人乳头瘤病毒(HPV)癌蛋白干扰的宿主分子已被证明是宫颈癌发生的潜在生物标志物,是细胞学检测和HPV检测的一种替代或补充手段。已知miR-203及其靶标之一ΔNp63是相互作用以控制角质形成细胞增殖和分化的宿主分子;二者在许多癌症中均被发现表达失调。由于p63和miR-203在宫颈癌发生中的作用尚未完全明确,因此,我们决定评估二者在宫颈癌发生过程中的表达变化。
本研究通过获取宫颈活检组织的定量聚合酶链反应(qPCR)数据来进行。
miR-203和ΔNp63在宫颈组织中呈现相似的表达模式,且二者在低级别鳞状上皮内病变(LSIL)与高级别鳞状上皮内病变(HSIL);HSIL与癌症之间均显示出统计学上的显著差异。此外,我们并未观察到ΔNp63 mRNA与miR-203水平如预期的负相关,而是在宫颈组织中呈正相关。
尽管是初步研究,但ΔNp63 mRNA和miR-203的表达水平似乎有望用于宫颈癌筛查。此外,miR-203与ΔNp63表达之间的正相关表明可能存在一些间接途径。然而,需要进一步研究来阐明ΔNp63和miR-203在宫颈癌发生中的作用,从而确定它们如何应用于新的诊断策略。