Expression of heavy subunit of γ-glutamylcysteine synthetase (γ-GCSh) in human colorectal carcinoma

Gamma-glutamylcysteine synthetase (gamma -GCS) is a heterodimer consisting of heavy (gamma -GCSh) and light (gamma -GCSI) subunits. gamma -GCS catalyzes the rate-limiting de novo biosynthesis of glutathione (GSH), an abundant physiological antioxidant that plays important roles for regulating oxidative stress. Expression of gamma -GCSh and gamma -GCSI are sensitive to oxidative stress. To investigate whether expression of gamma -GCS is correlated with tumor progression, we used immunohistochemical approaches to examine 16 human colorectal adenomas and resected 57 carcinomas from untreated patients. In adjacent normal colorectal epithelium, levels of gamma -GCSh expression were low. Strong cytoplasmic staining for gamma -GCSh was detected in 3 (18.8%) adenoma and 48 (84.2%) carcinomas. The frequency of gamma -GCSh expression in carcinoma was significantly higher than in adenoma (p < 0.0001). We used RNase protation assay and Western blot to determine levels of gamma -GCSh mRNA and protein from 10 pairs of matched carcinomas with adjacent normal controls. Elevated expression of both gamma -GCSh mRNA and protein were found in 6 cases, suggesting that transcriptional and for posttranscriptional regulation play an important role in the upregulation of gamma -GCS during colorectal carcinogenesis. We also examined the expression of another redox-regulated gene, multidrug resistance protein I (MRPI). Strong staining for MRPI was detected in I (6.3%) adenoma and 40 (70.2%) carcinomas. The frequency of MRPI expression in carcinoma was significantly higher than in adenoma ( p < 0.0001). Nuclear p53 expression was detected in 30 (52.6%) of carcinomas. There is a significant correlation between gamma -GCSh and MRP I expression (p = 0.013) but not between gamma -GCSh and p53. Since gamma -GCS is a sensor of oxidative stress, these results are consistent with the notion that oxidative stress is associated with colorectal tumor progression. (C) 2002 Wiley-Liss, Inc.