Evidence mapPaperPMID 41477177Full record

ReviewDrug design, development and therapy2025

SGLT2 Inhibitors in Combination Therapies for Tumors: A Novel Approach to Synergistic Treatment Strategies.

Hao Su, Xiangyu Li, Shurong Wang, Xuping Yang, Longyang Jiang, Hengli Luo, Yaping Li, Jie Zhou, Yilan Huang, Min Li

Abstract readReview
In one paragraph

Review in Drug design, development and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

10 authors.

Hao Su *Department of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Xiangyu Li *Department of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Shurong Wang *Department of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Xuping YangDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Longyang JiangDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.ORCID 0000-0002-8991-1446
Hengli LuoDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Yaping LiDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Jie ZhouDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Yilan HuangDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Min LiDepartment of Pharmacy, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-glucose cotransporter 2 (SGLT2) inhibitors, originally developed for glycemic control in type 2 diabetes, have shown potential therapeutic effects in cancer treatment. Studies suggest that SGLT2 inhibitors can suppress tumor growth and proliferation through the modulation of metabolic reprogramming in tumor cells, inhibition of tumor glucose uptake, and regulation of the tumor microenvironment. Recent studies have emphasized the potential benefits of combining SGLT2 inhibitors with conventional anticancer therapies, including chemotherapy (CT), immunotherapy, and targeted therapies. Several clinical trials are currently evaluating the safety and efficacy of these combinations. Both preclinical and clinical studies primarily explore the effectiveness of SGLT2 inhibitors in inhibiting tumor growth, reducing metastasis, and enhancing treatment outcomes. Identifying combination therapies with SGLT2 inhibitors could enable more personalized treatment selection and optimization. This review provides a comprehensive summary of the antitumor effects and underlying mechanisms of SGLT2 inhibitors when combined with conventional anticancer therapies, aiming to elucidate their emerging role in cancer treatment. Combination regimens involving SGLT2 inhibitors have the prospect to overcome certain limitations of monotherapy, offering promising clinical benefits and improving patient outcomes.

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsNeoplasmsSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsAnimalsCell ProliferationHumansAntineoplastic AgentsSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 Inhibitorsanticancer therapyantineoplastic agentscombination therapySGLT2 inhibitorstumor metabolism

Identifiers

PMID41477177
PMCPMC12751339

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.