Loss of Fhit expression as a potential marker of malignant progression in preinvasive squamous cervical cancer

David Butler, Claire Collins, Mohamed Mabruk, Mary B. Leader, Elaine W. Kay

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Objective. In a previous study using the same cases of squamous cervical neoplasia and microinvasive carcinoma (MICA) we found an association between FHIT gene deletion and infection with high-risk HPV (HR HPV). The purpose of this study was to evaluate Fhit protein expression by immunohistochemistry in order to determine whether FHIT gene deletion or infection with HR HPV correlated with aberrant protein expression and grade of lesion. Methods. A total of 74 archival LLETZ biopsy cases consisting of 23 cervical intraepithelial neoplasia grade 1 (CIN1), 28 CIN3, and 23 MICA cases were selected for Fhit immunostaining. The results of this study on Fhit immunostaining were analyzed in relation to our previous findings using Epi-Info and SPSS-PC statistical analysis software. Results. Fifty percent (14/28) of CIN3 lesions and 78% (18/23) of MICA lesions had a marked reduction or absence of Fhit protein expression (P = <0.001, strength of association, Cramers' V, 0.632). CIN1 lesions were found to have moderate to strong cytoplasmic expression of Fhit. Seventy percent of cases in this study with reduced/absent Fhit protein expression were also positive for FHIT gene loss of heterozygosity (LOH) (P = 0.04, strength of association, φ, 0.254). A significant statistical relationship was found between Fhit protein expression and HPV 16 infection in combined CIN1, CIN3, and MICA cases (P = <0.001). Eighty-seven percent of cases with reduced/absent Fhit protein expression were positive for HPV 16 (strength of association, φ, 0.552). Ninety percent of HPV 16 and 31 positive cases had reduced/absent Fhit expression. Conclusion. Our findings suggest an association between HPV infection and FHIT gene abnormalities raising the possibility of a mechanistic role for the FHIT gene as a cofactor with HPV in triggering the development of cervical cancer.

Original languageEnglish
Pages (from-to)144-149
Number of pages6
JournalGynecologic Oncology
Volume86
Issue number2
DOIs
Publication statusPublished - 2002

Fingerprint

Uterine Cervical Neoplasms
Cervical Intraepithelial Neoplasia
Human papillomavirus 16
Carcinoma
Proteins
Gene Deletion
Infection
Human papillomavirus 31
Genes
Loss of Heterozygosity
Software
Immunohistochemistry
Biopsy
Neoplasms

Keywords

  • Cervical cancer
  • FHIT gene
  • Fhit protein
  • HPV
  • LOH

ASJC Scopus subject areas

  • Oncology
  • Obstetrics and Gynaecology

Cite this

Loss of Fhit expression as a potential marker of malignant progression in preinvasive squamous cervical cancer. / Butler, David; Collins, Claire; Mabruk, Mohamed; Leader, Mary B.; Kay, Elaine W.

In: Gynecologic Oncology, Vol. 86, No. 2, 2002, p. 144-149.

Research output: Contribution to journalArticle

Butler, David ; Collins, Claire ; Mabruk, Mohamed ; Leader, Mary B. ; Kay, Elaine W. / Loss of Fhit expression as a potential marker of malignant progression in preinvasive squamous cervical cancer. In: Gynecologic Oncology. 2002 ; Vol. 86, No. 2. pp. 144-149.
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abstract = "Objective. In a previous study using the same cases of squamous cervical neoplasia and microinvasive carcinoma (MICA) we found an association between FHIT gene deletion and infection with high-risk HPV (HR HPV). The purpose of this study was to evaluate Fhit protein expression by immunohistochemistry in order to determine whether FHIT gene deletion or infection with HR HPV correlated with aberrant protein expression and grade of lesion. Methods. A total of 74 archival LLETZ biopsy cases consisting of 23 cervical intraepithelial neoplasia grade 1 (CIN1), 28 CIN3, and 23 MICA cases were selected for Fhit immunostaining. The results of this study on Fhit immunostaining were analyzed in relation to our previous findings using Epi-Info and SPSS-PC statistical analysis software. Results. Fifty percent (14/28) of CIN3 lesions and 78{\%} (18/23) of MICA lesions had a marked reduction or absence of Fhit protein expression (P = <0.001, strength of association, Cramers' V, 0.632). CIN1 lesions were found to have moderate to strong cytoplasmic expression of Fhit. Seventy percent of cases in this study with reduced/absent Fhit protein expression were also positive for FHIT gene loss of heterozygosity (LOH) (P = 0.04, strength of association, φ, 0.254). A significant statistical relationship was found between Fhit protein expression and HPV 16 infection in combined CIN1, CIN3, and MICA cases (P = <0.001). Eighty-seven percent of cases with reduced/absent Fhit protein expression were positive for HPV 16 (strength of association, φ, 0.552). Ninety percent of HPV 16 and 31 positive cases had reduced/absent Fhit expression. Conclusion. Our findings suggest an association between HPV infection and FHIT gene abnormalities raising the possibility of a mechanistic role for the FHIT gene as a cofactor with HPV in triggering the development of cervical cancer.",
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AB - Objective. In a previous study using the same cases of squamous cervical neoplasia and microinvasive carcinoma (MICA) we found an association between FHIT gene deletion and infection with high-risk HPV (HR HPV). The purpose of this study was to evaluate Fhit protein expression by immunohistochemistry in order to determine whether FHIT gene deletion or infection with HR HPV correlated with aberrant protein expression and grade of lesion. Methods. A total of 74 archival LLETZ biopsy cases consisting of 23 cervical intraepithelial neoplasia grade 1 (CIN1), 28 CIN3, and 23 MICA cases were selected for Fhit immunostaining. The results of this study on Fhit immunostaining were analyzed in relation to our previous findings using Epi-Info and SPSS-PC statistical analysis software. Results. Fifty percent (14/28) of CIN3 lesions and 78% (18/23) of MICA lesions had a marked reduction or absence of Fhit protein expression (P = <0.001, strength of association, Cramers' V, 0.632). CIN1 lesions were found to have moderate to strong cytoplasmic expression of Fhit. Seventy percent of cases in this study with reduced/absent Fhit protein expression were also positive for FHIT gene loss of heterozygosity (LOH) (P = 0.04, strength of association, φ, 0.254). A significant statistical relationship was found between Fhit protein expression and HPV 16 infection in combined CIN1, CIN3, and MICA cases (P = <0.001). Eighty-seven percent of cases with reduced/absent Fhit protein expression were positive for HPV 16 (strength of association, φ, 0.552). Ninety percent of HPV 16 and 31 positive cases had reduced/absent Fhit expression. Conclusion. Our findings suggest an association between HPV infection and FHIT gene abnormalities raising the possibility of a mechanistic role for the FHIT gene as a cofactor with HPV in triggering the development of cervical cancer.

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