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Original Research

Open Access

P16INK4a as a progression/regression tumour marker in LSIL cervix lesions: our clinical experience

  • S.G. Vitale1,*,
  • G. Valenti1
  • A.M.C. Rapisarda1
  • I. Calì1
  • I. Marilli1
  • M. Zigarelli1
  • G. Sarpietro1
  • A. Cianci1

1Department of General Surgery and Medical Surgical Specialties, University of Catania, Catania, Italy

DOI: 10.12892/ejgo3240.2016 Vol.37,Issue 5,October 2016 pp.685-688

Published: 10 October 2016

*Corresponding Author(s): S.G. Vitale E-mail: vitalesalvatore@hotmail.com

Abstract

Purpose of investigation: The aim of this prospective study was the evaluation of low-grade intraepithelial lesion (LSIL) lesions evolvement in woman with evidence of high risk HPV infection and p16INK4a negative expression. Materials and Methods: 150 women with cytological diagnosis of LSIL were selected to be underwent to three years of follow-up consisting in smear test, colposcopy, and protein p16INK4a investigation every six months and HPV-test every 12 months. Result: Final follow-up showed 45 cases of spontaneous lesion regression and 42 cases of persistence with absence of protein p16INK4a in all of them. There were three cases of disease progression to CIN2, two at 18-month follow-up and one at last follow-up. Disease progression was characterized of p16INK4a expression. Conclusion: p16INK4a should help to identify which LSIL cases are inclined to the progression of the disease and focalize which patients are eligible for specific treatment.

Keywords

Protein p16INK4a; LSIL; Marker of progression; High risk; HPV infection

Cite and Share

S.G. Vitale,G. Valenti,A.M.C. Rapisarda,I. Calì,I. Marilli,M. Zigarelli,G. Sarpietro,A. Cianci. P16INK4a as a progression/regression tumour marker in LSIL cervix lesions: our clinical experience. European Journal of Gynaecological Oncology. 2016. 37(5);685-688.

References

[1] Jemal A., Bray F., Center M.M., Ferlay J., Ward E., Forman D.: “Global cancer statistics”. CA Cancer J, Clin., 2011, 61, 69.

[2] Tota J.E., Chevarie-Davis M., Richardson L.A., Devries M., Franco E.L.: “Epidemiology and burden of HPV infection and related diseases: implications for prevention strategies”. Prev. Med., 2011, 53 Suppl 1, S12.

[3] Ma Y.Y., Cheng X.D., Zhou C.Y., Qiu L.Q., Chen X.D., Lü W.G., Xie X.: “Value of P16 expression in the triage of liquid-based cervical cytology with atypical squamous cells of undetermined significance and low-grade squamous intraepithelial lesions”. Chin. Med. J. (Engl.), 2011, 124, 2443.

[4] Galarowicz B., Jach R., Kidzierska J., Dyduch G., Zajac K., Pityński K., et al.: “The role of mRNA E6/E7 HPV high oncogenic risk expression in colposcopy of cervical intraepithelial neoplasia (CIN)”. Przegl. Lek., 2012, 69, 651.

[5] Benevolo M., Vocaturo A., Mottolese M., Mariani L., Vocaturo G., Marandino F., et al.: “Clinical role of p16INK4a expression in liquidbased cervical cytology: correlation with HPV testing and histologicdiagnosis”. Am. J. Clin. Pathol., 2008, 129, 606.

[6] McLaughlin-Drubin M.E., Park D., Munger K.: “Tumor suppressor p16INK4A is necessary for survival of cervical carcinoma cell lines”. Proc. Natl. Acad. Sci. U S A, 2013, 110, 16175.

[7] Tsoumpou I., Arbyn M., Kyrgiou M., Wentzensen N., Koliopoulos G., Martin-Hirsch P., 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, 210.

[8] Nieh S., Chen S.F., Chu T.Y., Lai H.C., Lin Y.S., Fu E., Gau C.H.: “Is p16(INK4A) expression more useful than human papillomavirus test to determine the outcome of atypical squamous cells of undetermined significance-categorized Pap smear? A comparative analysis using abnormal cervical smears with follow-up biopsies”. Gynecol. Oncol., 2005, 97, 35.

[9] Barcelos A.C., Michelin M.A., Adad S.J., Murta E.F.: “Atypical squamous cells of undetermined significance: Bethesda classification and association with Human Papillomavirus”. Infect. Dis. Obstet. Gynecol., 2011, 2011, 904674.

[10] Wentzensen N., Bergeron C., Cas F., Eschenbach D., Vinokurova S., von Knebel Doeberitz M.: “Evaluation of a nuclear score for p16INK4a-stained cervical squamous cells in liquid-based cytology samples”. Cancer, 2005, 105, 461.

[11] Arbyn M., Roelens J., Simoens C., Buntinx F., Paraskevaidis E., Martin-Hirsch P.P., Prendiville W.J.: “Human papillomavirus testing versus repeat cytology for triage of minor cytological cervical lesions”. Cochrane Database Syst. Rev., 2013, 3, CD008054.

[12] Lynge E., Rebolj M..: “Re: Age-specific evaluation of primary human papillomavirus screening vs conventional cytology in a randomized setting”. J. Natl. Cancer Inst., 2010, 102, 739.

[13] Eltoum I.A., Chhieng D.C., Roberson J., McMillon D., Partridge E.E.: “Reflex human papilloma virus infection testing detects the same proportion of cervical intraepithelial neoplasia grade 2-3 in young versus elderly women”. Cancer, 2005, 105, 194.

[14] Witkiewicz A.K., Knudsen K.E., Dicker A.P., Knudsen E.S.: “The meaning of p16(ink4a) expression in tumors: functional significance, clinical associations and future developments”. Cell Cycle, 2011, 10, 2497.

[15] Narisawa-Saito M., Kiyono T.: “Basic mechanisms of high-riskhuman papillomavirus-induced carcinogenesis: roles of E6 and E7 proteins”. Cancer Sci., 2007, 98, 1505.

[16] Ziemke P., Marquardt K., Griesser H.: “Predictive value of the combined p16 and Ki-67 immunocytochemistry in low-grade squamousintraepithelial lesions”. Acta Cytol., 2014, 58, 489.

[17] Carozzi F.M.: “Combined analysis of HPV DNA and p16INK4a expression to predict prognosis in ASCUS and LSIL pap smears”. Coll. Antropol., 2007, 31, 103.

[18] Agoff S.N., Lin P., Morihara J., Mao C., Kiviat N.B., Koutsky L.A.: “p16(INK4a) expression correlates with degree of cervical neoplasia: a comparison with Ki-67 expression and detection of high-risk HPV types”. Mod. Pathol., 2003, 16, 665.

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