Evidence map›Paper›PMID 41945221›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2026

Lactate and lactylation: metabolic architects of tumor progression and metastasis.

Hanyue Ma, Zhuo Gu, Zhenxin Wang

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Hanyue Ma *Department of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Zhuo Gu *Department of Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China.
Zhenxin WangDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China. zhenxw316@163.com.

Funding

National Natural Science Foundation of China 82473566
6 · The paper itself

Abstract

Lactate and its associated modification, lactylation, have emerged as key regulators in influencing various cellular processes. This review explores the multifaceted roles of lactate and lactylation, highlighting their involvement in metabolic reprogramming and the modulation of key signaling pathways. Lactate and lactylation influence cell adhesion, protein degradation, and angiogenesis, contributing to tumor invasion and metastasis. These metabolic alterations maintain cancer stem cell characteristics, support tumorigenesis and resistance to therapy. Lactate and lactylation also facilitate immune evasion in the tumor microenvironment (TME) by modulating immune cell function and immune checkpoint pathways. The complex interplay between lactate, lactylation, and various cellular and immune mechanisms underscores the potential of targeting lactate-related pathways as a therapeutic strategy for cancer treatment. Herein, we provide a comprehensive overview of the current understanding of lactate and lactylation in cancer, offering insights into their roles as key drivers of tumor progression and metastasis.

Indexed as

Disease ProgressionLactic AcidNeoplasmsAnimalsHumansMetabolic ReprogrammingNeoplasm MetastasisSignal TransductionTumor MicroenvironmentLactic Acid

Identifiers

PMID41945221
PMCPMC13057061

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.