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Targeting CD44s Molecule May Open New Door to Improved Cancer Therapies

Author:   Datetime:2017-07-21  Hits:

    Scientists at the Baylor College of Medicine have discovered that the molecule CD44s seems to give cancer cells a survival advantage. In the lab, eliminating this advantage by reducing the amount of CD44s resulted in cancer cells being more sensitive to the deadly effects of the drug erlotinib.


    The team’s study (“Internalized CD44s Splice Isoform Attenuates EGFR Degradation by Targeting Rab7A”) is published in the Proceedings of the National Academy of Sciences.




    “CD44 has been postulated as a cell surface coreceptor for augmenting receptor tyrosine kinase (RTK) signaling. However, how exactly CD44 triggers RTK-dependent signaling remained largely unclear,” write the investigators. “Here we report an unexpected mechanism by which the CD44s splice isoform is internalized into endosomes to attenuate EGFR [epidermal growth factor receptor] degradation. We identify a CD44s-interacting small GTPase [guanosine triphosphatase], Rab7A, and show that CD44s inhibits Rab7A-mediated EGFR trafficking to lysosomes and subsequent degradation.”


    "Treatment with erlotinib attempts to kill cancer cells by inhibiting EGFR signaling, a cellular mechanism that is hyperactive in most cases of glioblastoma multiforme and associated with poor prognosis," said senior author  Chonghui Cheng, M.D., Ph.D., associate professor of molecular and human genetics and of molecular and cellular biology at Baylor. "However, the clinical benefit of treatment with this and other EGFR inhibitors has been limited by the development of drug resistance."


    Erlotinib can inhibit EGFR signaling but in time cancer cells become resistant to the treatment, in part because other molecules can compensate for the lack of EGFR activity. Increasing evidence also suggests that EGFR and related signaling mechanisms do not act alone. Another molecule present in a number of cancers, CD44s, seems to be involved in sustaining those cancer-promoting mechanisms, but how this happens remained a mystery.


    "In this study, we discovered a mechanism by which CD44s helps maintain the EGFR signaling activated in glioblastoma multiforme," said Dr. Cheng, who also is a professor in the Lester and Sue Smith Breast Center at Baylor, part of the NCI-designated Dan L Duncan Comprehensive Cancer Center. "Working with a number of cancer cells grown in the lab, we determined that CD44s on the cell surface can enter the cell and prevent the digestion of EGFR, thus sustaining the activity of the signaling cascade that gives the cells a survival advantage."


    Dr. Cheng and her colleagues have shown that CD44s holds a strategic place from which it can influence not only EGFR but also a number of other signaling cascades that are important for cancer cell survival.


    "If we remove CD44s from the cell surface, we also can reduce the appearance of other molecules that could help cancer cells sustain their growth by compensating for the lack of EGFR activity," added Dr. Cheng.


    From the therapeutic point of view, the researchers also found that removing CD44s from cancer cells in culture and treating them with erlotinib resulted in higher cancer cell deaths than treating with erlotinib alone. The scientists anticipate that CD44s might also play a similar role in other types of cancer in which EGFR signaling is involved. This opens the possibility that targeting CD44s could potentially reduce the growth of many types of cancer, not just glioblastoma.


    "Researchers have been focused on developing inhibitors of EGRF and related pathways. Instead, we want to find novel approaches to boost the activity of inhibitors already available, and removing CD44s is a good example of how this could be done," said co-author Sali Liu, a graduate student in the Cheng lab. "Our work suggests that in the future, physicians and scientists might approach cancer treatment in a different way. For example, instead of deciding on a treatment based on the type of breast cancer a patient has, they might choose a treatment according to the type of mechanism that helps this particular cancer grow, regardless of the type of cancer it is."

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