Publications by authors named "Caitlyn Hyde"

Article Synopsis
  • Targeting transcription replication conflicts can reduce DNA damage and instability, offering new opportunities for cancer treatment.* -
  • AOH1996, a small molecule PCNA inhibitor, selectively induces cancer cell death by disrupting PCNA's function in DNA repair and enhancing its interaction with RNA polymerase II.* -
  • AOH1996 shows potential as a safe, orally administered cancer therapy that slows tumor growth, either alone or in combination with other treatments.*
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Tumor tropic neural stem cells (NSCs) can improve the anti-tumor efficacy of oncovirotherapy agents by protecting them from rapid clearance by the immune system and delivering them to multiple distant tumor sites. We recently completed a first-in-human trial assessing the safety of a single intracerebral dose of NSC-delivered CRAd-Survivin-pk7 (NSC.CRAd-S-pk7) combined with radiation and chemotherapy in newly diagnosed high-grade glioma patients.

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Background: Immortalized, clonal HB1.F3.CD 21 human neural stem/progenitor cells (NSCs), loaded with therapeutic cargo prior to intraperitoneal (IP) injection, have been shown to improve the delivery and efficacy of therapeutic agents in pre-clinical models of stage III ovarian cancer.

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Despite improvements in surgical techniques and chemotherapy, ovarian cancer remains the most lethal gynecologic cancer. Thus, there is an urgent need for more effective therapeutics, particularly for chemo-resistant peritoneal ovarian cancer metastases. Oncolytic virotherapy represents an innovative treatment paradigm; however, for oncolytic viruses tested from the last generation of genetically engineered viruses, the therapeutic benefits have been modest.

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