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DNA flow cytometry on human epidermis. The effect of serial biopsy sampling at various times
The British Journal of Dermatology
|July 1, 1982
Summary
Serial biopsy sampling significantly alters cell cycle fractions in leg ulcer patients within 24 hours. Previous biopsy injury impacts S-phase, while G2+M phase variation relates to daily rhythms, suggesting local and systemic effects.
Area of Science:
- Oncology
- Dermatology
- Cell Biology
Background:
- Leg ulcers are chronic wounds requiring frequent monitoring.
- Biopsy sampling is a common diagnostic tool.
- Understanding biopsy effects on cellular processes is crucial for accurate patient assessment.
Purpose of the Study:
- To investigate the impact of serial biopsy sampling on cell cycle distribution in lower abdominal skin of leg ulcer patients.
- To differentiate between short-term (within 24 hours) and longer-term (consecutive days) effects of biopsy sampling.
- To explore the relationship between biopsy-induced injury and cell cycle phase variations.
Main Methods:
- Single-nuclei DNA flow cytometry was employed to analyze cell cycle fractions (S-phase and G2+M phase).
- Four biopsies were taken at equal intervals within 24 hours from leg ulcer patients.
- A separate cohort underwent four biopsies taken at noon on consecutive days.
Main Results:
- Significant differences in S- and G2+M-fractions were observed in biopsies taken within 24 hours.
- No significant differences were found in biopsies taken on consecutive days at the same time.
- S-fraction variation correlated with biopsy-induced injury; G2+M variation showed a diurnal pattern.
Conclusions:
- Serial biopsy sampling within a 24-hour period can induce measurable changes in cell cycle kinetics.
- The timing and frequency of biopsies are critical factors influencing cellular responses.
- Biopsy procedures may exert both local and systemic effects on patient tissues, impacting cell proliferation markers.