HEALTH

Breaking the Cancer Code: New Hope for ER+ Breast Cancer

Sat Feb 22 2025
Breast cancer is a big deal, and a lot of it is estrogen receptor-positive (ER+). This means the cancer cells grow when they're exposed to estrogen. Doctors have been fighting this type of cancer for a while, and they've made some good progress. But, there are still some tough cases, like when the cancer spreads or doesn't respond to usual treatments. Scientists have found something interesting. There's a protein called USP7 that's really active in ER+ breast cancer. It helps the cancer grow and spread. If scientists can find a way to stop USP7, they might be able to slow down or even stop the cancer. Here's where it gets even more interesting. USP7 has a friend called CDK1. They work together to keep the cancer going. If scientists can block both USP7 and CDK1, they might be able to stop the cancer from growing and spreading. Scientists did some tests and found that when they blocked both USP7 and CDK1, the cancer stopped growing and spreading. This is a big deal because it means there might be a new way to treat ER+ breast cancer, especially in cases where the cancer has spread or doesn't respond to usual treatments. But, there's still a lot of work to do. Scientists need to figure out how to safely block USP7 and CDK1 in people. They also need to make sure that blocking these proteins doesn't cause other problems. This research is exciting because it gives hope to people with ER+ breast cancer. But, it's important to remember that this is just one step in a long journey. Scientists still have a lot of work to do before this can be used to treat people.

questions

    How does the inhibition of USP7 activity specifically induce apoptosis in estrogen receptor-positive breast cancer (ERPBC) cells?
    What are the long-term effects of combined inhibition of USP7 and CDK1 on overall patient health and quality of life?
    What are the potential side effects of targeting USP7 and CDK1, and how can they be mitigated in clinical settings?

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