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AstraZeneca looks to DNA damage-response drugs for edge in oncology | BioPharma Dive

Dive Brief: - AstraZeneca will be unveiling its DNA damage-response (DDR) research at the upcoming American Society of Clinical Oncology (ASCO) meeting next month, according to Reuters. - According to CEO Pascal Soriot, DDR is an emerging field in oncology and

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Dive Brief:

  • AstraZeneca will be unveiling its DNA damage-response (DDR) research at the upcoming American Society of Clinical Oncology (ASCO) meeting next month, according to Reuters.
  • According to CEO Pascal Soriot, DDR is an emerging field in oncology and one where AstraZeneca hopes to lead the way before other companies develop similar therapeutics.
  • One example of DDR that will be highlighted at ASCO is a therapy combining AstraZeneca's ovarian cancer drug Lynparza with an WEE1 inhibitor.

Dive Insight:

AstraZeneca has had to deal with a flurry of patent expirations on top-selling drugs, including its heartburn drug, Nexium, which generated roughly $3 billion per year at its height.

However, AstraZeneca is focused on investing in oncology to drive revenues in the future. Lynparza, the only FDA-approved PARP inhibitor has made a strong impact on the market for ovarian cancer treatment, and according to AstraZeneca, represents the forefront of the DDR therapeutics movement.

Going forward, AstraZeneca is looking not only to pioneer DDR therapeutics, but to also break into immuno-oncology. Bristol-Myers Squibb and Merck have already captured significant market share with their drugs Opdivo and Keytruda. AstraZeneca, meanwhile, has pegged its hopes to a combination therapy which pairs durvalumab and tremelimumab, according to Reuters.

But durvalumab hit a setback in December after trial results failed to support submission for approval as a monotherapy.

Overall, AstraZeneca continues to work feverishly to carve out a space in the growing oncology space---which is projected to be worth $175 billion by 2020. Higher revenues from cancer drugs could help the company reach its lofty goal of generating $45 billion per year in revenues by 2023.

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Evidence from Research

While more large-scale human trials are needed, several studies highlight Shilajit's protective effects: In Vitro Studies• Cells treated with fulvic acid show reduced DNA strand breaks• Markers of oxidative stress decline when exposed to Shilajit extracts Animal Studies• Rodents supplemented with Shilajit exhibit less DNA oxidation in liver tissues• Enhanced activity of superoxide dismutase (SOD) and glutathione peroxidase, two key antioxidant enzymes Clinical Observations• Preliminary trials suggest better energy levels and reduced markers of oxidative stress in healthy adults• Anecdotal reports of improved recovery after environmental toxin exposure

Source: ubiehealth.com ↗

Research Highlights

Several peer-reviewed studies illustrate NMN's impact on DNA repair: Animal Models Mice supplemented with NMN showed improved DNA repair markers in liver and muscle tissues. Young and aged mice both benefited, though aged mice saw the most dramatic improvements in sirtuin activity. Cell Culture Studies Human cells treated with NMN exhibited faster resolution of DNA strand breaks after exposure to UV light or oxidative stress. Increased NAD+ directly correlated with higher SIRT6 recruitment to damage sites. Early Human Trials Phase I studies report that daily NMN supplementation safely raises blood NAD+ levels by 30–70%. Participants displayed improved insulin sensitivity and markers of vascular health, indirectly supporting cellular repair processes. While long-term, large-scale human trials are still underway, the consistency across models has convinced many clinicians of NMN's promise in bolstering DNA repair.

Source: ubiehealth.com ↗
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Peptide Therapy Guide Editorial Team

Editorial team for Peptide Therapy Guide.

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