p16ink4a and HPV L1 Immunohistochemistry is Helpful for Estimating the Behavior of Low-grade Dysplastic Lesions of the Cervix Uteri

被引:97
作者
Negri, Giovanni [1 ]
Bellisano, Giulia [2 ]
Zannoni, Gian Franco [3 ]
Rivasi, Francesco
Kasal, Armin [1 ]
Vittadello, Fabio [4 ]
Antoniazzi, Sonia [1 ]
Faa, Gavino [2 ]
Ambu, Rossano [2 ]
Egarter-Vigl, Eduard [1 ]
机构
[1] Cent Hosp, Dept Pathol, I-39100 Bolzano, Italy
[2] Univ Cagliari, Sect Anat Pathol, Dept Cytomorphol, Cagliari, Italy
[3] Univ Cattolica Sacro Cuore, Dept Pathol, Fac Med Agostino Gemelli, I-00168 Rome, Italy
[4] Explora, Res & Stat Anal, Padua, Italy
关键词
p16; HPV; L1; cervical dysplasia; biologic behavior;
D O I
10.1097/PAS.0b013e3181709fbf
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
As only a minority of low-grade dysplastic lesions of the cervix uteri will eventually progress to carcinoma, predicting the behavior of these lesions could be of high value in clinical practice. The aim of the Study was to evaluate p 16(ink4a) and L1 as immunohistochemical markers of the biologic potentiality of low-grade dysplasia of the uterine cervix. The Study included 38 conization specimens with coexisting cervical intraepithelial neoplasia grade 1 (CIN1) and 3 (CIN3) (group A) and 28 punch biopsies from women with CIN1 and proven spontaneous regression in the follow-up (group B). In group A, all CIN3 were p(16ink4a) positive (p16+) and L1 negative (L1 -). The CIN1 of this group were p16+L1 - and p16+L1+ in 68.42%, and 31.57%, respectively. No other expression pattern was found in this group. In group B, the p16+L1-, p16+ L1 +, p16 - L1 +, and p16 - L1 - patterns were found in 3.57%, 25%, 14.29%, and 57.14%, respectively. Overall, 96.29% p16 + L1 - CIN1 were found in group A, whereas all the p16-L1+ and p16-L1- CIN1 were found in group B. A significant difference between staining pattern distributions of group A and B was observed (P < 0.0001). The results of the Study show that p16(ink4a) and L1 immunohistochemistry call be helpful for estimating the biologic potentiality of low-grade squamous cervical lesions. Particularly in cases in which the grade of the lesion is morphologically difficult to assess, the p16/L1 expression pattern Could be useful for planning the clinical management of these women.
引用
收藏
页码:1715 / 1720
页数:6
相关论文
共 18 条
[1]   p16INK4a expression correlates with degree of cervical neoplasia:: A comparison detection of high-risk with Ki-67 expression and HPV types [J].
Agoff, SN ;
Lin, P ;
Morihara, J ;
Mao, C ;
Kiviat, NB ;
Koutsky, LA .
MODERN PATHOLOGY, 2003, 16 (07) :665-673
[2]   Detection and typing of human papillomavirus DNA in uterine cervices with coexistent grade I and grade III intraepithelial neoplasia: biologic progression or independent lesions? [J].
Agorastos, T ;
Miliaras, D ;
Lambropoulos, AF ;
Chrisafi, S ;
Kotsis, A ;
Manthos, A ;
Bontis, J .
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2005, 121 (01) :99-103
[3]   Immunohistochemical expression of p16INK4a is predictive of HR-HPV infection in cervical low-grade lesions [J].
Benevolo, M ;
Mottolese, M ;
Marandino, F ;
Vocaturo, G ;
Sindico, R ;
Piperno, G ;
Mariani, L ;
Sperduti, I ;
Canalini, P ;
Donnorso, RP ;
Vocaturo, A .
MODERN PATHOLOGY, 2006, 19 (03) :384-391
[4]   New markers for cervical dysplasia to visualise the genomic chaos created by aberrant oncogenic papillomavirus infections [J].
Doeberitz, MV .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (17) :2229-2242
[5]   The papillomavirus life cycle [J].
Doorbar, J .
JOURNAL OF CLINICAL VIROLOGY, 2005, 32 :S7-S15
[6]  
Griesser H, 2004, ANAL QUANT CYTOL, V26, P241
[7]   Ki-67, cyclin E, and p16INK4 are complimentary surrogate biomarkers for human papilloma virus-related cervical neoplasia [J].
Keating, JT ;
Cviko, A ;
Riethdorf, S ;
Riethdorf, L ;
Quade, BJ ;
Sun, DQ ;
Duensing, S ;
Sheets, EE ;
Munger, K ;
Crum, CP .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (07) :884-891
[8]   p16INK4a immunohistochemistry improves interobserver agreement in the diagnosis of cervical intraepithelial neoplasia [J].
Klaes, R ;
Benner, A ;
Friedrich, T ;
Ridder, R ;
Herrington, S ;
Jenkins, D ;
Kurman, RJ ;
Schmidt, D ;
Stoler, M ;
Doeberitz, MV .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (11) :1389-1399
[9]   Overexpression of p16ink4a as a specific marker for dysplastic and neoplastic epithelial cells of the cervix uteri [J].
Klaes, R ;
Friedrich, T ;
Spitkovsky, D ;
Ridder, R ;
Rudy, W ;
Petry, U ;
Dallenbach-Hellweg, G ;
Schmidt, D ;
Doeberitz, MV .
INTERNATIONAL JOURNAL OF CANCER, 2001, 92 (02) :276-284
[10]   Immunocytochemical detection of HPV high-risk type L1 capsid proteins in LSIL and HSIL as compared with detection of HPV L1 DNA [J].
Melsheimer, P ;
Kaul, S ;
Dobeck, S ;
Bastert, G .
ACTA CYTOLOGICA, 2003, 47 (02) :124-128