Infrequent mutation of the H-cadherin gene on chromosome 16q24 in human breast cancers

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Abstract

To investigate the molecular basis of altered expression of the H-cadherin gene, we used polymerase chain reaction-single strand conformation polymorphism and DNA sequencing to examine the H-cadherin gene in 48 primary breast cancers in which loss of the long arm of chromosome 16 had been detected. We identified no mutations other than somatic 5-bp deletion within the coding region in a single tumor. The very low frequency of mutation found in these experiments suggests that H-cadherin is usually not a primary target for carcinogenesis in human breast cancers, and that reduction of its expression is likely to be a consequence of some other genetic event(s).

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Miki, Y., Katagiri, T., & Nakamura, Y. (1997). Infrequent mutation of the H-cadherin gene on chromosome 16q24 in human breast cancers. Japanese Journal of Cancer Research, 88(8), 701–704. https://doi.org/10.1111/j.1349-7006.1997.tb00439.x

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