Evidence map›Paper›PMID 42627059›Full record

ArticleOncology reports2026

Combination of lonidamine with devimistat induces synergistic antitumor effects in lung cancer via multifaceted disruption of cellular energy metabolism.

Xinhe Bai, Yongfeng Yang, Yuling Luo, Pei Jing, Xia Hong, Yaqin Zou, Yan Dai, Xuping Yang, Meiling Zhou, Han Xiao and 3 more

Abstract read
In one paragraph

Article in Oncology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Xinhe Bai *Department of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Yongfeng Yang *Department of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Yuling LuoDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Pei JingDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Xia HongDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Yaqin ZouDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Yan DaiDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Xuping YangDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Meiling ZhouDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Han XiaoDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Yilan HuangDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Shiwei GuoDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Qingze FanDepartment of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disrupting energy metabolic pathways has emerged as a promising strategy for cancer therapy including non‑small cell lung cancer (NSCLC). However, the ultimate anticancer effects have not been satisfactory. This is likely because cellular energy metabolism encompasses multiple processes and pathways, and tumor cells can flexibly regulate these processes and pathways to adapt to external disturbances and changes in the microenvironment in order to maintain their growth and proliferation. As a result, current strategies which only target certain aspects of energy metabolism have not achieved commendable results. In the present study, two inhibitors lonidamine and devimistat, each with their own limitations, were combined to treat A549 NSCLC by synergistically interfering with the main aspects of cellular energy metabolism including glycolysis, the tricarboxylic acid cycle and oxidative phosphorylation. The synergistic potency was examined

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungEnergy MetabolismIndazolesLung NeoplasmsA549 CellsAdenosine TriphosphateAnimalsApoptosisCaprylatesCell Line, TumorCell ProliferationCitric Acid CycleDrug SynergismGlycolysisHumansAdenosine TriphosphateCaprylatesdevimistatIndazoleslonidamineReactive Oxygen SpeciesSulfidescombination therapydevimistatglycolysislonidaminenon‑small cell lung canceroxidative phosphorylationtricarboxylic acid cycle

Identifiers

PMID42627059
PMCPMC13504670

What Socratic holds

Textmetadata
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.