A high ratio of apoptosis to proliferation correlates with improved survival after radiotherapy for cervical adenocarcinoma

Mary T. Sheridan, Rachel A. Cooper, Catharine M L West

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Purpose: A retrospective study was made of the role of apoptosis in determining radiotherapy outcome in 39 adenocarcinoma of the cervix. A comparison was also made of the detection of apoptosis by morphology and the TdT dUtp nick end-labeling (TUNEL) assay. Methods and Materials: The level of apoptosis was assessed in paraffin-embedded sections by cell morphology, the TUNEL assay, and a combination of the two. A total of 2,000 cells were counted per section, to obtain apoptotic (AI) and mitotic (MI) indices. Results: Patients with a high AI had a higher survival rate than those with a low AI, however, the difference was not significant. Using a ratio of apoptosis to proliferation indices, patients with an AI:MI > median had significantly better survival than those with AI:MI <median. This was true where the AI was quantified by morphology alone (p = 0.030) or in combination with the TUNEL assay (p = 0.008). Where the AI was quantified by a combination of morphology and TUNEL, the 5-year survival rates for women with AI:MI greater or less than the median were 81% and 25%, respectively. Conclusion: A high ratio of AI:MI in adenocarcinoma of the cervix indicates a good prognosis. A combination of the TUNEL assay and morphology provided the best discrimination between outcome groups.
    Original languageEnglish
    Pages (from-to)507-512
    Number of pages5
    JournalInternational Journal of Radiation Oncology Biology Physics
    Volume44
    Issue number3
    DOIs
    Publication statusPublished - 1 Jun 1999

    Keywords

    • Apoptosis
    • Cervix
    • Proliferation
    • Survival
    • TUNEL

    Fingerprint

    Dive into the research topics of 'A high ratio of apoptosis to proliferation correlates with improved survival after radiotherapy for cervical adenocarcinoma'. Together they form a unique fingerprint.

    Cite this