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Fluorescence in situ hybridization (FISH) Protocol in Human Sperm
Published on: September 1, 2009
Frequency of minisatellite repeat number changes at the MS205 locus in human sperm before and after cancer
N Zheng1, D G Monckton, G Wilson
1Department of Experimental Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Abstract:
To determine whether the measurement of repeat number mutations at a minisatellite locus could detect human germline mutations induced by chemotherapy, we performed a longitudinal study of the mutation frequencies in sperm from 10 patients treated for Hodgkin's disease. Polymerase chain reaction on small pools of DNA equivalent to 100 sperm and Southern blotting were used to screen at least 7900 sperm in each sample to quantify the mutation frequency at the minisatellite MS205 locus. Pretreatment and posttreatment semen samples were obtained at least 2 months after completion of therapy from 4 patients treated with a regimen (Novantrone, Oncovin, vinblastine and prednisone [NOVP]) that lacks alkylating agents and from three patients treated with regimens (Cytoxan, vinblastine, procarbazine and prednisone/Adriamycin, bleomycin, dacarbazine, lomustine, and prednisone [CVPP/ABDIC] or mechlorethamine, Oncovin, procarbazine and prednisone [MOPP]) containing alkylating agents. There were no effects of NOVP or CVPP/ABDIC on the mutation frequencies. In the 1 patient treated with MOPP, the treatment with the highest dose of gonadotoxic alkylating agents, there was a statistically significant increase in mutation frequency from 0.79% pretreatment to 1.14% posttreatment, indicating induction of mutations in stem spermatogonia. During-treatment semen samples obtained from 2 patients treated with ABVD, which does not contain gonadotoxic alkylating agents, and 1 with NOVP also did not show any increases above the baseline mutation frequencies, indicating no increase in the minisatellite mutation frequency in spermatocytes. Thus, measurement of repeat number changes at minisatellite MS205 appears to be able to detect induced germline mutations in human sperm. However, most chemotherapy regimens do not significantly increase this class of mutations.
Insights
Chemotherapy can induce germline mutations in human sperm, detectable by minisatellite mutation analysis. However, most treatments do not significantly increase these mutations, except for MOPP regimens containing alkylating agents.
Area of Science:
- Genetics
- Reproductive Biology
- Toxicology
Background:
- Chemotherapy is a crucial cancer treatment but can induce genetic damage.
- Assessing chemotherapy's impact on human germline mutations is vital for reproductive health.
- Minisatellite loci are sensitive markers for detecting DNA mutations.
Purpose of the Study:
- To evaluate if minisatellite mutation frequency in human sperm can detect chemotherapy-induced germline mutations.
- To investigate the mutagenic potential of different chemotherapy regimens on sperm DNA.
Main Methods:
- Longitudinal study of 10 Hodgkin's disease patients undergoing chemotherapy.
- Quantification of mutation frequency at the minisatellite MS205 locus using polymerase chain reaction and Southern blotting on sperm DNA.
- Analysis of pre- and post-treatment semen samples from patients receiving various chemotherapy regimens (NOVP, CVPP/ABDIC, MOPP).
Main Results:
- No significant increase in mutation frequency was observed in patients treated with NOVP or CVPP/ABDIC regimens.
- A statistically significant increase in mutation frequency (0.79% to 1.14%) was detected in one patient treated with the MOPP regimen, indicating induced mutations in stem spermatogonia.
- During-treatment samples from patients on ABVD or NOVP showed no increase in mutation frequency in spermatocytes.
Conclusions:
- Measurement of repeat number changes at minisatellite MS205 can detect chemotherapy-induced germline mutations in human sperm.
- Most chemotherapy regimens do not significantly elevate minisatellite mutation rates.
- The MOPP regimen, containing gonadotoxic alkylating agents, demonstrated mutagenic potential in human sperm stem cells.

