The Correct answer is B
![Accommodating risk: Responses to BRCA1/2 genetic testing of women who have had cancer [An article from: Social Science & Medicine]](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_tqOW24eYWW0X6xK_aPW4MgpCp7YMBe7ZTYO3kbLqZOp30i7kV--inaPpPwn8BWKbnxTsb9GcEKgUgdHobZrqbUSVuGQYAiJHxn2qwmkcYUesd0ANjwzln-dSVTxIEscGdG0LA7HehUXYcoxyS9HU-1zSxKZEVw5cCSXOx5ml8yQLXZ1N-s2w7x6B7UukjHfeol2FKGFil8eYOx4r3L0_XwePhF7e-85cUtvoWrqg=s0-d)
BRCA 1 & BRCA 2 cause early breast cancer (dominant inheritance). ATM gene causes breast cancer

– DNA repair disorder (recessive inheritance). P53 mutations are found in ~60% of all human cancer types including breast. Note Li-Frumeni syndrome – vulnerable to a wide range of cancers, 50% likelihood of Ca by age 30 & 90% by age 65. The precise function of p53 is unknown – may act as DNA policeman to prevent transcription & replication of unstable DNA.
Bcl-2 is involved in the control of apoptosis (programmed cell death) & prevents the p53 mediated destruction of cells with damaged DNA. It also may prevent the death of cells severely damaged by chemotherapy, & mediates drug resistance & contributes to neoplasia by this mechanism rather than promoting aberrant cell growth. It was first identified because of an association with follicular lymphoma.
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