Evidence mapPaperPMID 41942753Full record

Trial reportEMBO molecular medicine2026

The anti-obesogenic metabolite, Lac-Phe, is elevated by metformin treatment in prostate cancer patients.

Marijo Bilusic, Durga Prasad Gannamedi, Bhipasha Challu, Shomita Ferdous, Beatriz Mateo-Victoriano, Sheela Pokharel, Defne Bayik, Janaki Sharma, David B Lombard, Priyamvada Rai

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in EMBO molecular medicine, 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

10 authors.

Marijo BilusicDepartment of Medicine, Division of Medical Oncology, University of Miami Miller School of Medicine, Miami, FL, USA. mxb2305@med.miami.edu.ORCID 0000-0003-1020-689X
Durga Prasad GannamediDepartment of Pathology & Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL, USA.
Bhipasha ChalluCollege of Arts and Sciences, University of Miami, Coral Gables, FL, USA.ORCID 0009-0001-2787-1303
Shomita FerdousDepartment of Radiation Oncology, Division of Biology, University of Miami Miller School of Medicine, Miami, FL, USA.
Beatriz Mateo-VictorianoDepartment of Radiation Oncology, Division of Biology, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0003-3281-4933
Sheela PokharelDepartment of Radiation Oncology, Division of Biology, University of Miami Miller School of Medicine, Miami, FL, USA.
Defne BayikSylvester Comprehensive Cancer Center, Miami, FL, USA.ORCID 0000-0002-4740-8869
Janaki SharmaDepartment of Medicine, Division of Medical Oncology, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0001-7177-4319
David B LombardSylvester Comprehensive Cancer Center, Miami, FL, USA. dbl68@med.miami.edu.ORCID 0000-0002-4292-0185
Priyamvada RaiSylvester Comprehensive Cancer Center, Miami, FL, USA. prai@med.miami.edu.ORCID 0000-0001-7822-7553

Funding

Tumor Biology Research ProgramP30CA240139 · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · 2025 to 2025
$3.0M
Targeting the longevity regulator PAPP-A with small molecule inhibitorsR33AG077856 · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 2025 to 2025
$457k
SIRT5 inhibitors and degraders as novel treatments for Ewing sarcomaR01CA253986 · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · 2025 to 2025
$0k
Florida Department of Health (DOH) 24B12HHS | NIH | National Cancer Institute (NCI) P30CA240139HHS | NIH | National Cancer Institute (NCI) R01CA253986HHS | NIH | National Cancer Institute (NCI) R01CA254100HHS | NIH | National Institute on Aging (NIA) R33AG077856Melanoma Research Alliance (MRA) 1434401U.S. Department of Defense (DOD) ME200030U.S. Department of Veterans Affairs (VA) I01BX006593
6 · The paper itself

Abstract

Randomized clinical trials have highlighted the importance of weight control and exercise in improving cancer outcomes, yet the molecular mediators of these benefits remain poorly understood. Recent studies in Type 2 diabetic patients reported that the insulin-sensitizing drug, metformin, exerts its anorexigenic and anti-obesogenic effects through elevation of N-lactoyl-phenylalanine (Lac-Phe), a metabolite also reported to underlie the metabolic benefits of exercise in healthy individuals. Because metformin can be repurposed for oncology, we investigated whether the metformin/Lac-Phe link extends to cancer by profiling serum Lac-Phe levels in non-diabetic prostate cancer patients from BIMET-1, a prospective metformin trial, as well as those receiving metformin for metabolic dysfunction. Irrespective of disease stage, anticancer outcomes, or hormone therapy status, metformin treatment significantly and consistently increased serum Lac-Phe in these cancer patients to concentrations that approximated levels reported after strenuous exercise. Moreover, patients on the metformin arm of BIMET-1 exhibited improved weight management following anti-androgen therapy relative to those in the control group. By generalizing the metformin/Lac-Phe axis, our study provides a new molecular context for the metabolic benefits of repurposing metformin in cancer patients.

Indexed as

Hypoglycemic AgentsMetforminPhenylalanineProstatic NeoplasmsAgedHumansMaleMiddle AgedHypoglycemic AgentsMetforminN-lactoyl-phenylalaninePhenylalanineCancerHormone TherapyLac-PheMetforminWeight Management

Identifiers

PMID41942753
PMCPMC13179383

What Socratic holds

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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 Socratic graph.