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P16 as a marker of carcinoma in effusions and peritoneal washing.

Authors :
Carneiro FP
Amorim RF
de Vasconcelos Carneiro M
de Castro TMML
de Souza Vianna LM
Takano GHS
Daros AC
Peres I
Kuckelhaus SAS
Motoyama AB
Source :
BMC cancer [BMC Cancer] 2020 Mar 17; Vol. 20 (1), pp. 225. Date of Electronic Publication: 2020 Mar 17.
Publication Year :
2020

Abstract

Background: Considering the potential of p16 as a marker for diagnosis, prognosis and therapeutic response, the aim of this study was to assess its presence, via immunocytochemistry, in metastatic carcinoma of different primary sites and histological types obtained from effusions and peritoneal washings. A total of 118 samples including 85 of metastatic carcinoma and 33 samples of benign effusion/peritoneal washing were prepared by the plasma/thromboplastin method. Immunocytochemistry reactions were performed on cell block sections using antibodies against p16, claudin-4, MOC-31, calretinin, HBME and CD68.<br />Results: P16 overexpression was observed in 88.23% of all carcinoma samples. All cervix adenocarcinoma samples showed p16 overexpression. Overexpression in adenocarcinomas of ovary, lung and breast was observed in 93.75, 93.10 and 75% of the samples, respectively. Overexpression was observed in all different histological types analyzed: small cell carcinoma (lung), squamous cell carcinoma (cervical) and urothelial carcinoma (bladder). The specificity of p16 for carcinoma detection was of 96.96%.<br />Conclusion: Overexpression of p16 was observed in most metastatic carcinoma, from different primary sites and histological types, obtained from effusions and peritoneal washings. Due to its high frequency of overexpression in metastatic carcinoma, p16 may play a possible role in tumor progression and it may be considered as a complementary diagnostic marker depending on histological type and primary site of carcinoma.

Details

Language :
English
ISSN :
1471-2407
Volume :
20
Issue :
1
Database :
MEDLINE
Journal :
BMC cancer
Publication Type :
Academic Journal
Accession number :
32178642
Full Text :
https://doi.org/10.1186/s12885-020-6670-5