Antitumor activity of scorpion venom-derived peptides: A meta-analysis of preclinical studies.

Pharmacol ResAug 22, 2026 (epub)
Clinical ResearchOncology (Medical)

Lucero A Hernández-Carrizales, Alexa Hernández-Hernández, Jorge L Díaz-Gómez et al.

✦ AI-curated · Sources linked

In 30 seconds

This meta-analysis evaluated the antitumor effects of scorpion venom-derived peptides (SVDPs) across various cancer types in preclinical studies. A total of 27 articles were analyzed, revealing that SVDPs significantly reduced cell viability, particularly in lung cancer cells (IC 50 pooled mean: 12.69 μM; 95% CI: 5.80-19.57) and induced early apoptosis (SMD: 5.11; 95% CI: 2.54-7.68).

Key findings

  • SVDPs reduced cell viability in cancer cells, with a greater effect on lung cancer cells (IC 50 pooled mean: 12.69 μM; 95% CI: 5.80-19.57).
  • SVDPs induced early apoptosis with a standardized mean difference of 5.11 (95% CI: 2.54-7.68).
  • SVDPs reduced tumor volume in animal models (SMD = -7.29; 95% CI: -12.73 to -1.85).

Why it matters

Understanding the antitumor activity of SVDPs could lead to the development of novel cancer therapies that are more effective and selective, addressing current limitations in cancer treatment.

Source

Published in Pharmacol Res. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Oncology (Medical)

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.