TY - JOUR
T1 - Up-regulation of heat shock protein 27 in metaplastic and neoplastic lesions of the endocervix
AU - El-Ghobashy, AA
AU - Shaaban, AM
AU - Prime, W
AU - Innes, J
AU - Herrington, Charles Simon
PY - 2005/5
Y1 - 2005/5
N2 - Heat shock proteins (hsps) are molecular chaperones that are known to play a pivotal role in regulating intracellular homeostasis. hsp27 may have diagnostic and prognostic values for different gynecological malignancies. A cross-sectional analytical study was conducted at the Department of Pathology, The University of Liverpool, Liverpool, UK. Included in the study were 80 cervical glandular lesions of various histologic types, representing tuboendometrial metaplasia/endometriosis (n= 19), cervical glandular intraepithelial neoplasia (n= 33), and invasive adenocarcinoma (n= 28). Paraffin-embedded sections were stained using a commercial mouse monoclonal anti-hsp27 antibody with prior pressure-cooking for antigen retrieval. Sections of 11 normal cervices were used as controls. The median percentage of cells expressing hsp27 in each group was calculated. Normal cervical glands showed minimal expression of hsp27 (median: 10%, interquartile ranges [IQ]: 5-15). Expression was significantly more widespread in tuboendometrial metaplasia/endometriosis (median: 35%, IQ: 15-80), cervical glandular intraepithelial neoplasia (median: 60%, IQ: 32-80), and invasive adenocarcinoma (median: 40%, IQ: 25-80) when compared with normal endocervix (P= 0.007, < 0.001, and 0.001, respectively). However, no significant difference in hsp27 protein expression was found between cervical glandular intraepithelial neoplasia and invasive adenocarcinoma. In invasive adenocarcinoma, hsp27 showed no correlation with tumor grade, lymph node involvement, and lymphovascular space invasion. Our data highlight early dysregulation of hsp27 expression in both metaplastic and neoplastic lesions of the cervix.
AB - Heat shock proteins (hsps) are molecular chaperones that are known to play a pivotal role in regulating intracellular homeostasis. hsp27 may have diagnostic and prognostic values for different gynecological malignancies. A cross-sectional analytical study was conducted at the Department of Pathology, The University of Liverpool, Liverpool, UK. Included in the study were 80 cervical glandular lesions of various histologic types, representing tuboendometrial metaplasia/endometriosis (n= 19), cervical glandular intraepithelial neoplasia (n= 33), and invasive adenocarcinoma (n= 28). Paraffin-embedded sections were stained using a commercial mouse monoclonal anti-hsp27 antibody with prior pressure-cooking for antigen retrieval. Sections of 11 normal cervices were used as controls. The median percentage of cells expressing hsp27 in each group was calculated. Normal cervical glands showed minimal expression of hsp27 (median: 10%, interquartile ranges [IQ]: 5-15). Expression was significantly more widespread in tuboendometrial metaplasia/endometriosis (median: 35%, IQ: 15-80), cervical glandular intraepithelial neoplasia (median: 60%, IQ: 32-80), and invasive adenocarcinoma (median: 40%, IQ: 25-80) when compared with normal endocervix (P= 0.007, < 0.001, and 0.001, respectively). However, no significant difference in hsp27 protein expression was found between cervical glandular intraepithelial neoplasia and invasive adenocarcinoma. In invasive adenocarcinoma, hsp27 showed no correlation with tumor grade, lymph node involvement, and lymphovascular space invasion. Our data highlight early dysregulation of hsp27 expression in both metaplastic and neoplastic lesions of the cervix.
KW - cervix
KW - glandular neoplasia
KW - hsp27
KW - HEAT-SHOCK-PROTEIN
KW - UTERINE CERVIX
KW - RECEPTOR STATUS
KW - TUMOR-CELLS
KW - EXPRESSION
KW - HSP27
KW - CANCER
KW - ADENOCARCINOMA
KW - ENDOMETRIUM
KW - ESTROGEN
UR - http://www.blackwell-synergy.com/doi/abs/10.1111/j.1525-1438.2005.15316.x
U2 - 10.1111/j.1525-1438.2005.15316.x
DO - 10.1111/j.1525-1438.2005.15316.x
M3 - Article
SN - 1048-891X
VL - 15
SP - 503
EP - 509
JO - International Journal of Gynecological Cancer
JF - International Journal of Gynecological Cancer
ER -