We have previously shown that deficiency in the biotransformation enzyme glutathione-S-transferase theta (GSTT1) is a risk factor for multiple myeloma (MM). The present case-control study of 102 MM patients and 205 controls revealed a significant trend in increasing risk of MM with inheritance of mu
Caspase polymorphisms and genetic susceptibility to multiple myeloma
β Scribed by H. Dean Hosgood III; Dalsu Baris; Yawei Zhang; Yong Zhu; Tongzhang Zheng; Meredith Yeager; Robert Welch; Shelia Zahm; Stephen Chanock; Nathaniel Rothman; Qing Lan
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 87 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0278-0232
- DOI
- 10.1002/hon.852
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Multiple myeloma is a haematological malignency, characterized by clonal expansion of plasma cells. However, little is known about the cause of multiple myeloma. Cancer cells must avoid apoptosis to ensure unregulated tumour formation and growth. The highly conserved caspase cascade is essential to the regulation of the apoptotic pathway. To examine if five single nucleotide polymorphisms (SNPs) in four caspase genes [CASP3 Ex8β280 Cβ>βA (rs6948), CASP3 Ex8β+β567 Tβ>βC (rs1049216), CASP8 Ex14β271 Aβ>βT (rs13113), CASP9 Ex5β+β32 Gβ>βA (rs1052576), CASP10 Ex3β171 Aβ>βG (rs39001150)] alter multiple myeloma risk, we conducted a populationβbased caseβcontrol study of women (128 cases; 516 controls) in Connecticut. Compared to individuals with the TT genotype of CASP3 Ex8β+β567 Tβ>βC, subjects with the CC genotype had a fiveβfold decreased risk of multiple myeloma (odds ratio (OR)~CC~β=β0.2, 95% confidence interval (CI)β=β0.0β1.0). Further, individuals with the AG and AA genotypes of CASP9 Ex5β+β32 Gβ>βA also experienced a decreased risk of multiple myeloma (OR~AG~β=β0.8, 95% CIβ=β 0.5β1.3; OR~AA~β=β0.5, 95% CIβ=β0.3β0.9; pβtrendβ=β0.02). While no previous study has evaluated the association between caspase genes and multiple myeloma, studies have found associations with lung, breast, esophageal, gastric, colorectal and cervical cancers. Our parallel study of nonβHodgkin lymphoma, which utilized the same controls, found strong evidence that caspase genes play a key role in lymphogenesis. The protective associations observed in two key caspase genes suggest that genetic variation in CASP genes may play an important role in the aetiology of multiple myeloma. Copyright Β© 2008 John Wiley & Sons, Ltd.
π SIMILAR VOLUMES
## Communicated by Stephen Chanock Caspase-8 (CASP8) and caspase-10 (CASP10) play key roles in regulating apoptosis, and their functional polymorphisms may alter apoptosis and cancer risk. However, no reported studies have investigated the association between such polymorphisms and the risk of cut