Evidence map›Paper›PMID 36778600›Full record

ReviewFrontiers in endocrinology2022

Lactate-related metabolic reprogramming and immune regulation in colorectal cancer.

Qianhui Sun, Jingyuan Wu, Guanghui Zhu, Tingting Li, Xiaoyu Zhu, Baoyi Ni, Bowen Xu, Xinyi Ma, Jie Li

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

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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

9 authors.

Qianhui SunOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Jingyuan WuOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Guanghui ZhuOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Tingting LiGraduate College, Beijing University of Traditional Chinese Medicine, Beijing, China.
Xiaoyu ZhuOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Baoyi NiOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Bowen XuOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xinyi MaOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Jie LiOncology Department, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in cellular metabolism involving fuel sources are well-known mechanisms of cancer cell differentiation in the context of carcinogenesis. Metabolic reprogramming is regulated by oncogenic signaling and transcriptional networks and has been identified as an essential component of malignant transformation. Hypoxic and acidified tumor microenvironment contributes mainly to the production of glycolytic products known as lactate. Mounting evidence suggests that lactate in the tumor microenvironment of colorectal cancer(CRC) contributes to cancer therapeutic resistance and metastasis. The contents related to the regulatory effects of lactate on metabolism, immune response, and intercellular communication in the tumor microenvironment of CRC are also constantly updated. Here we summarize the latest studies about the pleiotropic effects of lactate in CRC and the clinical value of targeting lactate metabolism as treatment. Different effects of lactate on various immune cell types, microenvironment characteristics, and pathophysiological processes have also emerged. Potential specific therapeutic targeting of CRC lactate metabolism is also discussed. With increased knowledge, effective druggable targets might be identified, with the aim of improving treatment outcomes by reducing chemoresistance.

Indexed as

Colorectal NeoplasmsLactic AcidCarcinogenesisCell Transformation, NeoplasticGlycolysisHumansTumor MicroenvironmentLactic Acidcolorectal cancerimmune responseimmunoregulationlactatemetabolic reprogramming

Identifiers

PMID36778600
PMCPMC9909490

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Registered trials

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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 OpenQuestion graph.