Your topics. New publications.

A compact browser notification when there’s something new. At most once a day — no account needed.

What interests you?

Optional and switchable off here at any time. We save your selected topics and device subscription; no email address is required. Privacy

Search the harborEN/DEAccount
Hallmarks of aging
Research brief

Bibliometric review maps anti-aging drug literature 2005–2025 and proposes prioritization framework

This bibliometric-guided, strategy-oriented review maps explicit anti-aging drug literature from 2005 to 2025, names historically influential compounds and proposes a framework for prioritizing candidate gerotherapeutics; it is a literature synthesis, not a clinical trial. [1]

Automatic summary · not editorially reviewed

The key findings

  1. The review maps explicit anti-aging drug literature from 2005 to 2025 using a bibliometric-guided, strategy-oriented approach. [1]

  2. The field is described as converging on three partially overlapping intervention axes, including senotherapeutics and nutrient-sensing gerotherapeutics. [1]

  3. The Top 10 anchors are prioritized by bibliometric prominence rather than clinical ranking. [1]

The source at a glance

Study type / format
Bibliometric-guided, strategy-oriented literature review (abstract)
Population / context
Explicit anti-aging drug literature published from 2005 to 2025
Summary based on
Study abstract
Original publication
June 28, 2026

Review scope: anti-aging drug literature 2005–2025

The review describes a shift in anti-aging pharmacology from early exploratory lifespan-extension studies toward a hallmark-informed, multi-level framework combining mechanistic, preclinical and translational evidence. Using a bibliometric-guided, strategy-oriented approach, it maps the explicit anti-aging drug literature from 2005 to 2025 and identifies historically influential compounds.

Supporting source [1]

Three proposed intervention axes and Top 10 anchors

The field is said to converge on three partially overlapping intervention axes: senotherapeutics targeting cellular senescence and SASP signaling; nutrient-sensing and metabolic gerotherapeutics modulating mTOR, AMPK, autophagy and mitochondrial adaptation; and homeostasis-restoring agents reinforcing redox, inflammatory and circadian resilience. The Top 10 anchors are prioritized by bibliometric prominence rather than clinical ranking and are said to illustrate both potential and limitations in human translation.

Supporting source [1]

Framework aims to guide future gerotherapeutic prioritization

The synthesis presents itself as a structured framework for interpreting historical and contemporary literature, clarifying the relationship between multi-hallmark engagement and functional outcomes, and guiding rational prioritization of candidate gerotherapeutics for future research. Emerging candidates and platform innovations are mentioned as ongoing progress toward precision geromedicine. The abstract reports no primary data, sample, follow-up or outcome results.

Supporting source [1]

How to interpret this

Abstract only; the full text was not reviewed. This is a bibliometric-guided literature review, not a clinical trial, and the abstract reports no sample, follow-up, outcome data or effect sizes. The Top 10 anchors reflect bibliometric prominence, not clinical efficacy, and translational readiness is discussed as a framework proposal rather than validated human benefit.

Based on the study abstract; the full paper, tables and supplementary data were not reviewed.

Source & supporting passages

[1]
From lifespan extension to hallmark-informed gerotherapeutic prioritization: A bibliometric-guided, strategy-oriented review of anti-aging drug research.

Liu Z, Abulaiti A, Li D, Li J, Wahafu P, Zhang Y, Maimaitiming M, Shu L, Li G, Yakufu M. · europepmc.org · June 28, 2026

Read the quoted passagesIn the language of the original source
  1. Finding 1 ↑

    from 2005 to 2025, identifies historically influential
  2. Finding 2 ↑

    three partially overlapping intervention axes
  3. Finding 3 ↑

    prioritized by bibliometric prominence rather than clinical

AI-assisted summary with linked source passages. No independent editorial or clinical review.

Our editorial method

Discussion

Community discussions

0 topics

Member contributions. Share sources, disclose commercial interests, and avoid personal medical or dosing advice.

Loading…