PCR-RFLP and FTIR-based detection of high-risk human papilloma virus for cervical cancer screening and prevention

Autor(es)

Alves Melo, Igor Martins ^[1] ; Pereira Viana, Magda Rogeria ^[1] ; Pupin, Breno ^[1] ; Bhattacharjee, Tanmoy Tapobrata ^[2] ; Canevari, Renata de Azevedo ^[1]

Afiliação do(s) autor(es)

^[1] Univ Vale Paraiba, Inst Pesquisa & Desenvolvimento, Lab Biol Mol Canc, UNIVAP, Ave Shishima Hifumi 2911, BR-12244000 Sao Paulo, SP - Brazil

^[2] Univ Otago, Sir John Walsh Res Inst, 310 Great King St, Dunedin 9016 - New Zealand

• Tipo de documento: Artigo Científico
• Fonte: BIOCHEMISTRY AND BIOPHYSICS REPORTS; v. 26, JUL 2021.
• Citações Web of Science: 0

Resumo

Background: Approximately 70% of cervical carcinoma cases show the presence of high-risk Human Papilloma Virus (HPV), especially HPV-16 and HPV-18, and can be used to stratify high risk patients from low risk and healthy. Currently, molecular biology techniques such as polymerase chain reaction (PCR) are used to identify the presence of virus in patient samples. While the methodology is highly sensitive, it is labor intensive and time-consuming. Alternative techniques, such as vibrational spectroscopy, has been suggested as a possible rapid alternative. Therefore, in this study, we evaluate the efficiency of cervical fluid Fourier Transform Infrared spectroscopy (FTIR) in patient risk stratification informed by PCR. Methods: Cervical fluid samples (n = 91) were obtained from patients who have undergone routine Papanicolaou (Pap) test. Viral genome was identified and classified as high/low-risk by PCR-Restriction Fragment Length Polymorphism (PCR-RFLP). FTIR spectra were acquired from samples identified by PCR-RFLP as No-HPV (n = 10), high-risk HPV (n = 7), and low-risk HPV (n = 7). Results: Of the 91 samples, was detected the viral genome by PCR in 36 samples. Of these 36 samples, nine samples were identified to contain high-risk HPV (HR-HPV) and nine samples were found to have low-risk HPV (LR-HPV). The FTIR spectra acquired from No-HPV, LR-HPV, and HR-HPV showed differences in 1069, 1437, 1555, 1647, 2840, 2919, and 3287 cm(-1) bands. Principal Component Analysis (PCA) showed distinct clusters for No-HPV and HR-HPV and No-HPV and LR-HPV, but there was significant overlap in the clusters of HR-HPV and LR-HPV. PCA-Linear Discriminant Analysis (PC-LDA) after Leave One Out Cross Validation (LOOCV) classified No-HPV from HR-HPV and No-HPV from LR-HPV with 100% efficiency in the 1400-1800 cm(-1) spectral range. LOOCV classifications for LR-HPV and HR-HPV from each other were 71 and 75%, respectively, in the 2800-3400 cm(-1) spectral range. Conclusions: The results highlight the high sensitivity of PCR-RFLP in HPV identification and show that FTIR can classify samples identified as healthy, low, and high-risk samples by PCR-RFLP. General significance: We show the possibility of using FTIR for initial cervical cancer risk stratification followed by detailed PCR-RFLP investigations for suspect cases. (AU)

• Processo FAPESP: 13/14464-9 - Caracterização molecular e bioquímica de lesões da tireóide para diagnóstico clínico
• Beneficiário: Renata de Azevedo Canevari
• Modalidade de apoio: Auxílio à Pesquisa - Regular