Introduction
The human glutathione S-transferases (GSTs) are a multigene, isoenzyme family. Cytosolic GST isoenzymes can be classified by their substrate specificities, isoelectric points and amino acid sequence homologies into major classes termed α, μ, π and θ, which are encoded by a superfamily of genes located at different loci [
1,
2]. There are currently five putative α class genes encoding subunits GSTA1, GSTA2, GSTA3, GSTA4 and GSTω, whereas the GST π class contains a single gene encoding the GSTP1 protein, and the θ class consists of two genes encoding the GSTT1 and GSTT2 proteins.
The
GSTM1 gene belongs to the GST μ class gene family, members of which are clustered on chromosome 1p13, and which contains five genes encoding subunits GSTM1, GSTM2, GSTM3, GSTM4 and GSTM5 [
3,
4]. The presence or absence of the
GSTM1 gene constitutes the polymorphism, and the lack of the
GSTM1 gene, which is caused by a gene deletion (the GSTM1-null genotype), affects approximately 50-60% of the population [
5,
6]. Homozygosity for the GSTM1-null genotype has been found to confer risk for many cancers, including those of the breast [
7,
8,
9,
10,
11,
12,
13,
14,
15,
16,
17]. The GSTM1-null genotype was positively associated with high DNA adduct levels, suggesting it has a role in carcinogenesis [
7]. Smokers with a GSTM1 deficiency had a significantly elevated risk for developing lung, laryngeal and bladder cancer [
8,
9]. The GSTM1-null genotype has also been associated with higher risk for environmentally related cancer, such as cancers of colon, head and neck, skin, oesophagus and stomach [
9,
10,
11,
12,
13].
For breast cancer, the GSTM1-null genotype has been found to confer an increased risk in young post-menopausal women [
14], whereas other studies did not find any association [
18,
19]. GST μ deletions have been reported to be associated with higher grade tumours [
15], however, and to confer accumulation of epoxides, which are mutagenic [
16]. GST isoenzymes catalyze the conjugation of glutathione to several electrophilic compounds, including polyaromatic hydrocarbon, which is lipophilic and stored in adipose tissues, such as those of the breast [
20]. Aromatic adducts were found to be higher in women with breast cancer than in healthy control individuals [
21]. Most polyaromatic compounds are metabolized to reactive epoxide intermediates by the polymorphic cytochrome p450 (CYP1AI) and detoxified by phase II enzymes, including GST. The variation in conjugation of epoxide substrate intermediates has been observed to segregate with inherited loss of the
GSTM1 gene. Therefore, individuals who inherit the homozygous form of the null polymorphism in the
GSTM1 gene will not be capable of conjugating and detoxifying specific substrate epoxide intermediates [
16]. In addition, a wide variety of alkylating chemotherapeutic agents used in the treatment of breast cancer have been postulated to act as substrates for the GSTM1 protein products, thus reducing the effectiveness of these agents as cytotoxins [
22].
In an attempt to further characterize the clinical features associated with the GSTM1-null genotype, we examined allelism at the GSTM1 locus in 92 locally advanced breast cancer patients undergoing primary chemotherapy. Allelism at the GSTM1 locus was analysed by polymerase chain reaction (PCR) in paired samples of blood and breast tissue. To determine whether levels of GSTM1 expression in patients with a positive genotype has a predictive or a prognostic value, RNA expression was measured by reverse transcription (RT)-PCR in breast tumour samples obtained before and after treatment. Results were then compared with clinicopathological factors of the patients, including characterization for
p53 gene mutations [
23], clinical response to chemotherapy, and disease-free and overall survival.
Materials and methods
Patients and samples
After an initial diagnostic biopsy, including characterization for p53 gene alterations, 92 women who were diagnosed with locally advanced breast carcinoma and who underwent primary chemotherapy were included in this study. The median clinical follow up was 78months (range 10-120months). Three of these patients had bilateral lesions, and in these three cases both lesions were examined. No family history for breast cancer was recorded in the 92 women. The patients received chemotherapy treatment (four or six courses, each lasting 21days) with a regimen containing cyclophosphamide, doxorubicine and 5-fluorouracil. The criteria for inclusion were as follows: inflammatory carcinomas, positive nodes and/or large (T3, T4) tumours. Clinical response to primary chemotherapy was categorized according to World Health Organization criteria and was considered as objective response (complete or partial response) or no response (stabilization or progression). In all cases neither radiotherapy nor hormone therapy were applied before chemotherapy.
Tumours were characterized before treatment by the clinical tumour size (categorized as T2, T3 or T4); the clinical nodal involvement (categorized as N0, N1 or N2); the histologic grade of Scarff, Bloom and Richardson (categorized as SBR1, SBR2 or SBR3); the hormone receptors (categorized as HR- or HR+, and considered as positive for oestrogen and/or progesterone receptors); the pathological tumour size (categorized as pT0, pT1, pT2 or pT3); and the number of involved axillary nodes (categorized as pN-, pN1+ and pN3+ for none, one or two, and three or more involved nodes, respectively).
Peripheral blood lymphocytes were obtained from each patient. Tumour samples were frozen in liquid nitrogen and stored at -80°C until analysis. Genomic DNA was extracted using proteinase, followed by phenol extraction and ethanol precipitation according to standard procedures [
24].
Polymerase chain reaction method
The GSTM1-null genotype was determined by coamplifi-cation with the interferon-β gene, which served as an internal control. Primers for amplification of the GSTM1 gene corresponding to exon 4, intron 5 and exon 5 were 5' -ctgccctacttgattgatggg-3' and 5' -ctggattgtagcagatcatgc-3' (amplified product size, 271 base pairs). Primers for amplification of a part of the interferon-β gene, producing a constant 170-base pair band in all samples, were 5' -ggcacaacaggtagtaggcg-3' and 5' -gccacaggagcttctgacac-3' . Because the primers for the GSTM1 locus anneal to sites inside the coding region of the gene, the presence of the gene was determined by the presence of the band, whereas the null-genotype was determined by the lack of the band, using agarose gel electrophoresis (2%).
PCR was performed using 250ng template DNA in 10mmol/l Tris-HCl (pH8.4), 50mmol/l potassium chloride, 1.5mmol/l magnesium chloride (Bioprobe Systems, Illkirch, France), 0.2mmol/l concentrations of each deoxynucleotide triphosphate (dNTP), 500nmol/l concentrations of each primer and 2.5units of Taq DNA polymerase (Bioprobe Systems). The reaction (total volume 50 μ l) was amplified on a Omnigene thermal cycler (Hybaid Ltd, Ashford, Kent, UK). After an initial denaturation at 94°C for 3 min the reaction proceeded for 25 cycles of 50s at 94°C, 50s at 55°C and 50s at 72°C, concluded by a final extension step of 10min at 72°C. To test for contamination, negative controls (tubes containing the PCR mixture without the DNA template) were included in every run.
Reverse transcription polymerase chain reaction
Total RNA was obtained by the acid guanidine thiocyanate-phenol-chloroform extraction method [
25]. Of the total RNA 1 μ g was dissolved in 20 μ l reverse transcriptase buffer (Gibco/BRL, Cergy Pontoise, France) containing 200 μ mol/l dNTP, 500 ng random hexamer and 200U avian myeloblastosis virus (AMV) reverse transcriptase (Superscript; Gibco/BRL). The reaction was incubated at 42°C for 50min and heated to 70°C for 15min.
The PCR reaction was carried out in a 50 μ l volume of PCR buffer (Promega, Madison, Wisconsin, USA) containing 200 μ mol/l dNTP, 2.5 μ l complementary DNA template, 2.5U Taq DNA polymerase, and 500nmol/l of bothGSTM1 and β
2- microglobulin primers. The reaction was initiated by a heat step at 95°C for 2min, and carried out for 25 cycles of denaturation at 94°C for 50s, annealing at 55°C for 50s and extension at 72°C for 50s. Blanks for each reaction were included with all samples. Of PCR product 10 μ l were analysed on a 2% agarose gel with ethidium bromide staining. Band intensities were determined with a gel doc 1000 UV system (Biorad, Ivry-Sur-Seine, France), and the ratio of GSTM1 to β
2- microglobulin was calculated.
Determination of p53 mutations
The determination of
p53 mutations was performed as previously described [
23]. Briefly, breast tumour samples were characterized before and after treatment for
p53 gene mutations by PCR single-strand confirmation polymorphism and/or direct sequencing of exons 5-9 of the
p53 gene.
Hormonal receptor assay
The oestrogen and progesterone receptor levels were determined in cytosolic tumours using enzyme immunoassay methods (Abbott Laboratories, Rungis, France). The cutoff level used for oestrogen and progesterone was 20fmol/mg cytosolic proteins.
Statistical analysis
The Pearson χ
2 test was used as a homogeneity test for proportion. A stepwise logistic regression model with the logoistic regression (LR)-BMDP program (University of California Press, Berkeley, California, USA) [
26] was used to assess the contribution of each independent factor to the GSTM1-null genotype and the probability of response to primary chemotherapy. The log-rank test using the Kaplan-Meier method was used to study the relationship between each factor and the probability of disease-free survival (median 50months) and overall survival (median 78months). A multivariate analysis using the Cox proportional hazards model was performed to assess the contribution of each independent factor to the probability of survival. For logistic regression or Cox regression models the enter and remove limits were 0.1 and 0.15, respectively. Overall significance of each factor (
P value) was given by the likelihood ratio test. Results are expressed as odds ratios (OR) and corresponding 95% confidence interval (CI), with the significance of ORs being derived from the ratio of the coefficient divided by its standard error (Wald test). Statistical analysis for RNA
GSTM1 expression was performed using the SAS/STAT program (SAS Institute Inc, Cary, North Carolina, USA) by using student
t-test or analysis of variance, Pearson χ
2 test and log-rank test. For all tests, optimality of the selected models was verified by all-possible-subsets analyses.
Discussion
In the present study, the frequency of
GSTM1 gene deficiency among breast carcinoma patients (57%) was similar to that previously reported in this lesion [
9,
14,
15,
16,
17,
18,
19]. Among individuals with GSTM1-positive genotype no deletion was observed in somatic tumour cells, suggesting that the deletion of
GSTM1 gene was not a characteristic of breast tumour cells.
Several series have determined that
GSTM1 deletions were involved in the aetiology of breast cancer [
9,
14,
17], whereas another studies did not find any such associations [
18,
19]. In addition, little is known about clinical characteristics that confer
GSTM1 deletion among breast cancer patients. Only one recently published study [
19] reported no relation between clinicopathological parameters and GSTM1 genotype in primary breast tumours. The results obtained in the present study are consistent with these data, because no differences were noted when a variety of known prognostic factors were compared between tumours from patients with and those without GSTM1-null genotype. These factors include age, menopausal status, clinical and pathological tumour size, clinical and pathological nodal involvement, pathological grade, hormone receptors status and
p53 gene mutations. These results suggest that clinical tumour features are not associated with GSTM1-null genotype, not only in primary breast cancers, but also in advanced breast cancers.
An improved survival has been observed in patients with GSTM1-null genotype and has been explained by a better response to chemotherapeutic agents related to more effective cell killing, which in turn is related to the absence of protective effect of GSTM1 allele [
18]. Among the most active chemotherapeutic agents in the treatment of breast cancer are cyclophosphamide and anthracyclines. These compounds are conjugated with thiols through reactions mediated by GST. The π class of transferase is thought to be the major factor involved in the subsequent prevention of DNA alkylation [
22], although there has been some suggestion that the μ class is also involved [
27]. In order to determine whether the absence of GSTM1 locus favours the response to chemotherapeutic agents, and whether, on the contrary, GSTM1-positive genotype may confer a resistance to chemotherapy, we analysed GSTM1 polymorphisms in relation to clinical response to chemotherapy. The results demonstrated that the objective response rate of the group with GSTM1-null genotype did not differ from those with GSTM1-positive genotype. Thus, individuals carrying the GSTM1 locus were no more resistant to chemotherapy than those with GSTM1-null genotype.
GSTM1 RNA expression levels measured in patients with positive genotype were also not associated with clinical response to chemotherapy. Among clinical parameters analysed, only clinical tumour size and the presence of intraductal carcinoma were found to influence clinical response to primary chemotherapy. The results also revealed that GSTM1-null genotype was not related to survival in advanced breast cancer patients, in contrast to the absence of hormone receptors and to the presence of
p53 gene mutations, which are known to be of prognostic value in advanced breast cancer [
28,
29,
30].
Although the group studied was not very large (n = 92), the clinical characteristics were well known and the results strongly suggest the lack of correlation of GSTM1-null genotype alone with prognostic factors, clinical reponse to chemotherapy and survival. Genotypes of other enzymes (CYP1A1, GSTT1), as well as combinations of genotypes, might be of interest with regard to cancer and carcinogen metabolism.
Taken together, these results show that advanced breast cancers arising in patients with GSTM1-null genotype have no worse clinical tumour charactaristics and outcome than those of patients without such deletions. Thus, the lack of correlation of GSTM1-null genotype with clinical tumour features, clinical response to chemotherapy and survival exclude a role for GSTM1 polymorphism as a prognostic factor in advanced breast cancer.