Literature DB >> 18095132

Analysis of immunohistochemical expression of p53 and the proliferation marker Ki-67 antigen in skull base chordomas: relationships between their expression and prognosis.

Keiichi Sakai1, Kazuhiro Hongo, Yuichiro Tanaka, Jun Nakayama.   

Abstract

The prognosis of chordomas is difficult to predict based solely on histological findings. The purpose of this study was to assess the immunohistochemical expression of the proliferation marker Ki-67 antigen and the expression of p53 in skull base chordomas and to relate their expressions to the outcome. We examined the expression of p53 and the MIB-1 labeling index (LI), assessed by Ki-67 expression, in 19 tumors (initial, n = 11; recurrent, n = 8) from 11 patients. The correlation among the MIB-1 LI, p53 expression, and the clinical outcome was analyzed. The mean MIB-1 LI and p53 expression at the initial surgery were 5.6 +/- 4.6% and 9.0 +/- 9.4%, respectively. At the time of recurrence, the mean MIB-1 LI and p53 expression were 10.2 +/- 7.4% and 16.5 +/- 12.0%. The correlation between the MIB-1 LI and p53 expression at the initial and recurrent surgeries was highly significant (r = 0.948; P < 0.0001). The change in p53 expression from the initial to the recurrent chordomas was significantly greater in patients who died of tumor-related causes than in the surviving patients. In the surviving patients, the values for MIB-1 LI and p53 expression in the recurrent tumors were significantly higher in the disease-ongoing group than in the disease-free group. Our results suggest that determination of the immunohistochemical expression of p53 and Ki-67 antigen is helpful to predict tumor recurrence and prognosis in skull base chordomas.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 18095132     DOI: 10.1007/s10014-007-0222-4

Source DB:  PubMed          Journal:  Brain Tumor Pathol        ISSN: 1433-7398            Impact factor:   3.298


  5 in total

1.  The prognostic value of Ki-67, p53, epidermal growth factor receptor, 1p36, 9p21, 10q23, and 17p13 in skull base chordomas.

Authors:  Craig Horbinski; Gerard J Oakley; Kathleen Cieply; Geeta S Mantha; Marina N Nikiforova; Sanja Dacic; Raja R Seethala
Journal:  Arch Pathol Lab Med       Date:  2010-08       Impact factor: 5.534

2.  In chordoma, metastasis, recurrences, Ki-67 index, and a matrix-poor phenotype are associated with patients' shorter overall survival.

Authors:  Adrian von Witzleben; Lukas T Goerttler; Jochen Lennerz; Stephanie Weissinger; Marko Kornmann; Regine Mayer-Steinacker; Alexandra von Baer; Markus Schultheiss; Peter Möller; Thomas F E Barth
Journal:  Eur Spine J       Date:  2015-09-23       Impact factor: 3.134

3.  Fascin expression in skull base chordoma: correlation with tumor recurrence and dura erosion.

Authors:  Ziyun Gao; Qiuhang Zhang; Feng Kong; Ge Chen; Mingchu Li; Hongchuan Guo; Jiantao Liang; Yuhai Bao; Feng Ling
Journal:  Med Oncol       Date:  2012-02-16       Impact factor: 3.064

Review 4.  The molecular aspects of chordoma.

Authors:  Sukru Gulluoglu; Ozlem Turksoy; Aysegul Kuskucu; Ugur Ture; Omer Faruk Bayrak
Journal:  Neurosurg Rev       Date:  2015-09-12       Impact factor: 3.042

Review 5.  Immunophenotypic features of dedifferentiated skull base chordoma: An insight into the intratumoural heterogeneity.

Authors:  Kelvin Manuel Piña Batista; Kenia Yoelvi Alvarez Reyes; Fátima Pérez Lopez; Andrés Coca Pelaz; Ivan Fernandez Vega; José Luis Llorente Pendás; Antonio Saiz Ayala; Aurora Astudillo; Jorge Andrés Nuñez Rojas; Patricia Barrio Fernandez
Journal:  Contemp Oncol (Pozn)       Date:  2017-12-30
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.