Common susceptibility genes for cancer: search for the end of the rainbowBMJ 2006; 332 doi: https://doi.org/10.1136/bmj.332.7550.1150 (Published 11 May 2006) Cite this as: BMJ 2006;332:1150
- Stuart G Baker, biostatistician ([email protected])1,
- Jaakko Kaprio, genetic epidemiologist2
- 1 National Cancer Institute, Bethesda MD 20892-7354, USA
- 2 University of Helsinki, Helsinki, Finland
- Correspondence to: S G Baker
- Accepted 9 March 2006
Huge resources are being invested in the search for common inherited genetic variants that increase susceptibility to cancer. However, these studies are expensive because they require large sample sizes to rule out false positive results (table).1 2 The US cancer genetic markers of susceptibility project (http://cgems.cancer.gov/), for example, will cost $14m (£7.9m; €11m). In addition, large replication studies may still be necessary to confirm generalisability to other populations. For these studies to eventually lead to a clinical therapeutic benefit, common genetic variants that increase susceptibility to cancer must exist and it must be feasible to rigorously evaluate the clinical benefit of targeting these common genetic variants. Both these requirements require formal consideration.
Common cancer susceptibility genes are unlikely
Devoting a large research effort to searching for common cancer susceptibility genes has several problems. The first is that recent research suggests these genes are unlikely to exist or, if they do, are unlikely to have much of an effect on the incidence of cancer. The early phases of carcinogenesis seem to entail alterations in the stroma (supporting tissue) rather than a genetic mutation of the parenchyma (functional tissue).3 4 Thus genetic susceptibility to cancer of the parenchyma (except for rare genes related to familial cancer) would have a relatively small role in the early stages of carcinogenesis. Moreover, a recent study could not find conclusive evidence of genetic alterations in the stroma,5 further diminishing the probable role of genetic susceptibility in early …
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