Breast Cancer Genes and Mutations

Breast cancer is cancer that develops from breast tissue. Signs of breast cancer may include a lump in the breast, a change in breast shape, dimpling of the skin, milk rejection, fluid coming from the nipple, a newly inverted nipple, or a red or scaly patch of skin. In those with distant spread of the disease, there may be bone pain, swollen lymph nodes, shortness of breath, or yellow skin.
Breast cancer most commonly presents as a lump that feels different from the rest of the breast tissue. More than 80% of cases are discovered when a person detects such a lump with the fingertips.
Another symptom complex of breast cancer is Paget's disease of the breast. This syndrome presents as skin changes resembling eczema; such as redness, discolouration or mild flaking of the nipple skin. As Paget's disease of the breast advances, symptoms may include tingling, itching, increased sensitivity, burning, and pain.
Breast cancer, like other cancers, occurs because of an interaction between an environmental (external) factor and a genetically susceptible host. Normal cells divide as many times as needed and stop. They attach to other cells and stay in place in tissues. Cells become cancerous when they lose their ability to stop dividing, to attach to other cells, to stay where they belong, and to die at the proper time.
Normal cells will self-destruct (programmed cell death) when they are no longer needed. Until then, cells are protected from programmed death by several protein clusters and pathways. One of the protective pathways is the PI3K/AKT pathway; another is the RAS/MEK/ERK pathway. Sometimes the genes along these protective pathways are mutated in a way that turns them permanently "on", rendering the cell incapable of self-destructing when it is no longer needed. This is one of the steps that causes cancer in combination with other mutations. Normally, the PTEN protein turns off the PI3K/AKT pathway when the cell is ready for programmed cell death. In some breast cancers, the gene for the PTEN protein is mutated, so the PI3K/AKT pathway is stuck in the "on" position, and the cancer cell does not self-destruct

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  • @Armistead_MacSkye
    @Armistead_MacSkye Жыл бұрын

    Excellent upload.

  • @michaeleisenberg7867
    @michaeleisenberg7867 Жыл бұрын

    Good Morning 🌄 Shabir, This is an excellent review 📖. Thank you very much. 👏👏👏🎄⛄🎁

  • @hussainbiology

    @hussainbiology

    Жыл бұрын

    My pleasure

  • @MK-agirlwhosmissunderstood
    @MK-agirlwhosmissunderstood10 ай бұрын

    What about the ZNF703 Gene? Thank you kindly

  • @umerfarooqbiology7083
    @umerfarooqbiology7083 Жыл бұрын

    hussain bro thanks to share knowledge

  • @hussainbiology

    @hussainbiology

    Жыл бұрын

    thanks bro

  • @mohammadsibtainkadri2887
    @mohammadsibtainkadri2887 Жыл бұрын

    Hi Sir These are some challenging questions (molecular cell biology) asked by my professor. I am unable to answer this. Could you please try these questions. 1. In a hypothetical single-cell eukaryote, SRP and translocon are both encoded by a single gene. Your friend plans to produce a secretory enzyme more efficiently by over-expressing SRP and translocon in these cells. Will this plan work? Why or why not? 6. As shown in Figure 14-8 (in the slides, the 6th ed.), Sar1 is a GTP binding protein involved in the formation (budding) of COPII vehicles. Predict the consequences if the Sar1 has a defect that results in the reduction of GTP-GDP swap efficiency. 3. Challenging questions: There are four kinds of pumps in page 447 (the 6thondition): P-class, V-class, F-class, and ABC superfamily. V- and F-class are similar in structure but different in function. What would you do if you want to “re-engineer the desired class into V-class? 5. Challenging question: The G-protein coupled receptors have seven trans-membrane domains. Can the number be reduced to three? Why or why not?

  • @roghayehijabi4707
    @roghayehijabi4707 Жыл бұрын

    Thank you 🎉🎊👏👏👏👌

  • @hussainbiology

    @hussainbiology

    Жыл бұрын

    Thank you too

  • @hezhamohamadpanah1161
    @hezhamohamadpanah11616 ай бұрын

    I really can't understand

  • @aaqibhameed2972
    @aaqibhameed2972 Жыл бұрын

    👏👍👍👏👏