Дополнительные диагностические возможности в практике ПАП-теста методом жидкостной цитологии

Автор: Аксаментов Артем Константинович, Мельникова Надежда Васильевна, Колышкина Надежда Александровна, Кучерова Ольга Николаевна, Баклаушев Владимир Павлович

Журнал: Клиническая практика @clinpractice

Рубрика: Обзоры

Статья в выпуске: 1 т.12, 2021 года.

Бесплатный доступ

Роль проонкогенных штаммов вируса папилломы человека в развитии рака шейки матки не вызывает сомнений. В настоящее время в программах скрининга рака шейки матки применяется стратегия котестирования, включающая цитологическое и ВПЧ-исследования, которые могут быть осуществлены одномоментно при помощи инновационного метода - жидкостной цитологии (ЖЦ). Новейшая технология позволяет проводить дополнительные диагностические генетические исследования, благодаря которым возможна более эффективная сортировка пациентов с целью оптимизации объема диагностических и лечебных мероприятий. В статье изучена эффективность диагностических тестов на основе оценки экспрессии микроРНК и мРНК, а также тестов на основе анализа метилирования ДНК по материалу ЖЦ. Внедрение в клиническую практику исследований новых молекулярно-генетических предикторов развития рака шейки матки расширяет возможности скрининговых программ, применяемых в настоящее время.

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Пап-тест, скрининг, рак шейки матки, микрорнк, мрнк, жидкостная цитология, метилирование днк

Короткий адрес: https://sciup.org/143175842

IDR: 143175842   |   DOI: 10.17816/clinpract64982

Список литературы Дополнительные диагностические возможности в практике ПАП-теста методом жидкостной цитологии

  • Wild CP, Weiderpass E, Stewart BW. World Cancer Report: Cancer Research for Cancer Prevention. Lyon, France: International Agency for Research on Cancer, 2020. Avalable from: https://www. iarc.who.int/featured-news/new-world-cancer-report/
  • Злокачественные новообразования в России в 2019 году (заболеваемость и смертность). Под ред. А.Д. Капри-на, В.В. Старинского, А.О. Шахзадовой. Москва: МНИОИ им. П.А. Герцена — филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2020. 252 с. [Malignant neoplasms in Russia in 2019 (morbidity and mortality). Ed. by A.D. Kaprin, V.V. Starinsky, A.O. Shakhzadova. Moscow: P.A. Herzen Moscow State Medical Research Institute-branch of the Federal State Budgetary Institution «NMIC of Radiology» of the Ministry of Health of Russia; 2020. 252 p. (In Russ).]
  • Клинические рекомендации. Цервикальная интраэпите-лиальная неоплазия, эрозия и эктропион шейки матки. Общероссийская общественная организация «Российское общество специалистов по профилактике и лечению опухолей репродуктивной системы», Российское общество акушеров-гинекологов, 2020. [Clinical recommendations. Cervical intraepithelial neoplasia, erosion and ectropion of the cervix. All-Russian public organization «Russian Society of Specialists in the Prevention and Treatment of Tumors of the Reproductive System», Russian Society of Obstetricians and Gynecologists; 2020. (In Russ).] Режим доступа: https://sudact.ru/law/klinicheskie-rekomendatsii-tservikalnaia-intraepitelialnaia-neoplaziia-eroziia-i/klinicheskie-rekomendatsii/. Дата обращения: 12.02.2021.
  • Rozemeijer K, Penning C, Siebers AG, et al. Comparing Sure-Path, ThinPrep, and conventional cytology as primary test method: SurePath is associated with increased CIN II + detection rates. Cancer Causes Control. 2016;27(1):15-25. doi: 10.1007/s10552-015-0678-1
  • De Oliveira AC, Domingues MF, Neufeld PM, et al. Comparison between Conventional Cytology and Liquid-Based Cytology in the Tertiary Brazilian Navy Hospital in Rio de Janeiro. Acta Cytol. 2020;64(6):539-546. doi: 10.1159/000508018
  • Taylor S, Kuhn L, Dupree W, et al. Direct comparison of liquid-based and conventional cytology in a South African screening trial. Int J Cancer. 2006;118(4):957-962. doi: 10.1002/ijc.21434
  • Comprehensive Cytopathology. 3th Edition. Bibbo M.D., Wilbur, Elsevier; 2008.
  • Hoda RS, VandenBussche C, Hoda SA. Liquid-Based Specimen Collection, Preparation, and Morphology. In: Hoda RS, VandenBussche C, Hoda SA, ed. Diagnostic Liquid-Based Cytology. Berlin, Heidelberg: Springer; 2017. Р. 1-12.
  • Whitlock EP, Vesco KK, Eder M, et al. Liquid-based cytology and human papillomavirus testing to screen for cervical cancer: a systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2011;155(10):687-697. doi: 10.7326/0003-4819-155-10-201111150-00376
  • Ho GY, et al. Natural history of cervicovaginal papillomavirus infection in young women. N Engl J Med. 1998;338(7):423-428. doi: 10.1056/NEJM199802123380703
  • Koliopoulos G, et al. Diagnostic accuracy of human papil-lomavirus testing in primary cervical screening: a systematic review and meta-analysis of non-randomized studies. Gynecol Oncol. 2007;104(1):232-246. doi: 10.1016/j.ygyno.2006.08.053
  • Mayrand MH, et al. Human papillomavirus DNA versus Papanicolaou screening tests for cervical cancer. N Engl J Med. 2007;357(16):1579-1588. doi: 10.1056/NEJMoa071430
  • Altobelli E, et al. HPV-vaccination and cancer cervical screening in 53 WHO European Countries: An update on prevention programs according to income level. Cancer Med. 2019;8(5):2524-2534. doi: 10.1002/cam4.2048
  • Leeman A, et al. Reliable identification of women with CIN3+ using hrHPV genotyping and methylation markers in a cytology-screened referral population. Int J Cancer. 2019;144(1):160-168. doi: 10.1002/ijc.31787
  • Schmitz M, et al. Performance of a methylation specific real-time PCR assay as a triage test for HPV-positive women. Clin Epigenetics. 2017;9. doi: 10.1186/s13148-017-0419-2
  • Arbyn M, et al. Evidence regarding human papillomavirus testing in secondary prevention of cervical cancer. Vaccine. 2012;30(Suppl 5):F88-99. doi: 10.1016/j.vaccine.2012.06.095
  • Bergeron C, et al. Prospective evaluation of p16/Ki-67 dual-stained cytology for managing women with abnormal Pa-panicolaou cytology: PALMS study results. Cancer Cytopathol. 2015;123(6):373-381. doi: 10.1002/cncy.21542
  • Lanner L, Lindström AK. Incidence of HPV and HPV related dysplasia in elderly women in Sweden. PloS One. 2020;15(3):e0229758. doi: 10.1371/journal.pone.0229758
  • Luttmer R, et al. p16/Ki-67 dual-stained cytology for detecting cervical (pre)cancer in a HPV-positive gynecologic outpatient population. Mod Pathol Off. J. U. S. Can Acad Pathol Inc. 2016;29(8):870-878. doi: 10.1038/modpathol.2016.80
  • Wentzensen N. et al. p16/Ki-67 Dual Stain Cytology for Detection of Cervical Precancer in HPV-Positive Women. JNCI J. Natl. Cancer Inst. 2015;107(12. doi: 10.1093/jnci/djv257
  • Wentzensen N, et al. Clinical Evaluation of Human Papillomavirus Screening With p16/Ki-67 Dual Stain Triage in a Large Organized Cervical Cancer Screening Program. JAMA Intern Med. 2019;179(7):881-888. doi: 10.1001/jamainternmed.2019.0306
  • Carozzi F, et al. Use of p16-INK4A overexpression to increase the specificity of human papillomavirus testing: a nested substudy of the NTCC randomised controlled trial. Lancet Oncol. 2008;9(10):937-945. doi: 10.1016/S1470-2045(08)70208-0
  • Ovestad IT, et al. Clinical value of fully automated p16/Ki-67 dual staining in the triage of HPV-positive women in the Norwegian Cervical Cancer Screening Program. Cancer Cytopathol. 2017;125(4):283-291. doi: 10.1002/cncy.21807
  • Colla^o LM, Zardo L. CHAPTER 3 - Cytologic Screening Programs. Comprehensive Cytopathology (Third Edition). Ed. Bibbo M., Wilbur D. Edinburgh: W.B. Saunders; 2008. Р. 47-57.
  • Jamison J, Wilson RT, Carson J. The evaluation of human papillomavirus genotyping in cervical liquid-based cytology specimens; using the Roche Linear Array HPV genotyping assay. Cytopathol Off J Br Soc Clin Cytol. 2009;20(4):242-248. doi: 10.1111/j.1365-2303.2009.00643.x
  • Sahebali S, et al. Immunocytochemistry in liquid-based cervical cytology: analysis of clinical use following a cross-sectional study. Int J Cancer. 2006;118(5):1254-1260. doi: 10.1002/ijc.21489
  • Bubendorf L. Multiprobe fluorescence in situ hybridization (UroVysion) for the detection of urothelial carcinoma - FISHing for the right catch. Acta Cytol. 2011;55(2):113-119. doi: 10.1159/000323652
  • Macfarlane LA, Murphy PR. MicroRNA: Biogenesis, Function and Role in Cancer. Curr Genomics. 2010;11(7):537-561. doi: 10.2174/138920210793175895
  • Iorio MV, Croce CM. Causes and consequences of mi-croRNA dysregulation. Cancer J Sudbury Mass. 2012;18(3):215-222. doi: 10.1097/PPO.0b013e318250c001
  • Ribeiro J, et al. miR-34a and miR-125b Expression in HPV Infection and Cervical Cancer Development. BioMed Res. Int. 2015;(2015):304584. doi: 10.1155/2015/304584
  • Malta M, et al. Let-7c is a Candidate Biomarker for Cervical Intraepithelial Lesions: A Pilot Study. Mol Diagn Ther. 2015;19(3):191-196. doi: 10.1007/s40291-015-0145-4
  • Tian Q, et al. MicroRNA detection in cervical exfoliated cells as a triage for human papillomavirus-positive women. J Natl Cancer Inst. 2014;106:9. doi: 10.1093/jnci/dju241
  • Lu J, et al. Regulation of Canonical Oncogenic Signaling Pathways in Cancer via DNA Methylation. Cancers. 2020;12:11. doi: 10.3390/cancers12113199
  • Tirado-Magallanes R, et al. Whole genome DNA methyla-tion: beyond genes silencing. Oncotarget. 2016;8(3):5629-5637. doi: 10.18632/oncotarget.13562
  • Mirabello L, et al. Elevated methylation of HPV16 DNA is associated with the development of high grade cervical intraepithelial neoplasia. Int J Cancer. 2013;132(6):1412-1422. doi: 10.1002/ijc.27750
  • Piyathilake CJ, et al. A higher degree of methylation of the HPV 16 E6 gene is associated with a lower likelihood of being diagnosed with cervical intraepithelial neoplasia. Cancer. 2011;117(5):957-963. doi: 10.1002/cncr.25511
  • Kottaridi C, et al. Quantitative Measurement of L1 Human Papillomavirus Type 16 Methylation for the Prediction of Preinvasive and Invasive Cervical Disease. J Infect Dis. 2017;215(5):764-771. doi: 10.1093/infdis/jiw645
  • Lorincz AT. Virtues and Weaknesses of DNA Methylation as a Test for Cervical Cancer Prevention. Acta Cytol. 2016;60(6):501-512. doi: 10.1159/000450595
  • Bonde J, et al. Methylation markers FAM19A4 and MIR124-2 as triage strategy for primary human papillomavirus screen positive women: A large European multicenter study. Int J Cancer. 2021;148(2):396-405. doi: 10.1002/ijc.33320
  • Leeman A, et al. Expression of p16 and HPV E4 on biopsy samples and methylation of FAM19A4 and miR124-2 on cervical cytology samples in the classification of cervical squamous intraepithelial lesions. Cancer Med. 2020;9(7):2454-2461. doi: 10.1002/cam4.2855
  • Dippmann C, et al. Triage of hrHPV-positive women: comparison of two commercial methylation-specific PCR assays. Clin Epigenetics. 2020;12. doi: 10.1186/s13148-020-00963-w
  • De Vuyst H, et al. Methylation Levels of CADM1, MAL, and MIR124-2 in Cervical Scrapes for Triage of HIV-infected, High-Risk HPV-Positive Women in Kenya. J Acquir Immune Defic Syndr. 2015;70(3):311-318. doi: 10.1097/QAI.0000000000000744
  • Kong L, et al. DNA methylation for cervical cancer screening: a training set in China. Clin Epigenetics. 2020;12. doi: 10.1186/s13148-020-00885-7
  • van Leeuwen RW, et al. DNA methylation markers as a triage test for identification of cervical lesions in a high risk human papillomavirus positive screening cohort. Int J Cancer. 2019;144(4):746-754. doi: 10.1002/ijc.31897
  • Kim MK, et al. DNA methylation in human papillomavirus-infected cervical cells is elevated in high-grade squamous intraepithelial lesions and cancer. J Gynecol Oncol. 2016;27:2. doi: 10.3802/jgo.2016.27.e14
  • Tsoumpou I, et al. p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis. Cancer Treat Rev. 2009;35(3):210-220. doi: 10.1016/j.ctrv.2008.10.005
  • Del Pino M, et al. mRNA biomarker detection in liquid-based cytology: a new approach in the prevention of cervical cancer. Mod Pathol Off J. U. S. Can Acad Pathol Inc. 2015;28(2):312-320. doi: 10.1038/modpathol.2014.106
  • Мельникова Н.В., Антонова И.Б., Бабаева Н.А., и др. Результаты выявления, типирования и количественного определения вируса папилломы человека методом ПЦР в практике жидкостной цитологии у женщин в постменопаузе // Вестник Российского научного центра рентгенрадиологии. 2020. Т. 20, № 4. С. 134-151. [Melnikova NV, Antonova IB, Babaeva NA, et al. Results of detection, typing and quantification of human papillomavirus by PCR in thepractice of liquid cytology in postmenopausal women. Bulletin of the Russian Scientific Center of Roentgenora-diology. 2020;20(4): 134-151. (In Russ).]
  • Wang HY, et al. Use of hTERT and HPV E6/E7 mRNA RT-qPCR TaqMan assays in combination for diagnosing highgrade cervical lesions and malignant tumors. Am J Clin Pathol. 2015;143(3):344-351. doi: 10.1309/AJCPF2XGZ2XIQYQX
  • Мельникова Н.В., Боженко В.К., Антонова И.Б., и др. Цер-викальные интраэпителиальные неоплазии: анализ профиля МРНК в практике жидкостной цитологии // Акушерство и гинекология. 2017. № 4. 95-100. [Melnikova NV, Bozhenko VK, Antonova IB, et al. Cervical intraepithelial neoplasia: analysis of mrna profile in the practice of liquid-based cytology. Obstetrics and gynegology. 2017;(4). 95-100. (In Russ).] doi: 10.18565/AIG.2017.4.95-100
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