Evidence map›Paper›PMID 41813913›Full record

ArticleScientific reports2026

Phytochemical profile and chemosensitizing anticancer activity of Mitragyna speciosa and mitragynine.

Panita Kongsila, Thidarut Boonmars, Pranee Sriraj, Jatuporn Prathumtet, Praphat Manuelo Ruengthanoo, Ratchadawan Aukkanimart

Abstract read
In one paragraph

Article in Scientific 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

6 authors.

Panita KongsilaDepartment of Thai Traditional Medicine, Faculty of Natural Resources, Rajamangala University of Technology Isan, Sakon Nakhon Campus, Sakon Nakhon, 47160, Thailand.ORCID http://orcid.org/0009-0007-5646-8381
Thidarut BoonmarsDepartment of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.ORCID http://orcid.org/0000-0002-7262-7190
Pranee SrirajDepartment of Thai Traditional Medicine, Faculty of Natural Resources, Rajamangala University of Technology Isan, Sakon Nakhon Campus, Sakon Nakhon, 47160, Thailand.ORCID http://orcid.org/0000-0003-2819-1016
Jatuporn PrathumtetDepartment of Thai Traditional Medicine, Faculty of Natural Resources, Rajamangala University of Technology Isan, Sakon Nakhon Campus, Sakon Nakhon, 47160, Thailand.ORCID http://orcid.org/0000-0003-2261-564X
Praphat Manuelo RuengthanooDepartment of Thai Traditional Medicine, Faculty of Natural Resources, Rajamangala University of Technology Isan, Sakon Nakhon Campus, Sakon Nakhon, 47160, Thailand.ORCID http://orcid.org/0009-0005-9547-0332
Ratchadawan AukkanimartDepartment of Thai Traditional Medicine, Faculty of Natural Resources, Rajamangala University of Technology Isan, Sakon Nakhon Campus, Sakon Nakhon, 47160, Thailand. ratchadawan.au@rmuti.ac.th.ORCID http://orcid.org/0000-0002-8041-3598

Funding

Thailand Science Research and Innovation Fundamental Fund 2024 (Project code 200772)
6 · The paper itself

Abstract

This study examined the phytochemical composition, antioxidant efficacy, and cytotoxic properties of Mitragyna speciosa (kratom) extracts and its principal alkaloid, mitragynine. The extracts exhibited significant antioxidant properties, and chemical analysis verified mitragynine as the principal alkaloid, aligning with the distinctive phytochemical profile of M. speciosa. In vitro cytotoxicity studies demonstrated that both kratom extract and mitragynine suppressed cancer cell proliferation (A549, KKU213C, and HeLa cancer cell lines) in a concentration- and time-dependent manner, with mitragynine displaying greater potency compared to the crude extract, especially against cholangiocarcinoma cells. Importantly, synergistic cytotoxic effects were noted when kratom extract or mitragynine was combined with standard chemotherapeutic agents across various cancer cell lines, especially HeLa cervical cancer. These effects correlated with diminished expression of the anti-apoptotic protein BCL-2. In general, the results show that M. speciosa extract and mitragynine are chemosensitizers that could make standard chemotherapy work better. Additional research is necessary to clarify the molecular mechanisms involved and to confirm these effects in vivo.

Indexed as

Antineoplastic Agents, PhytogenicMitragynaPhytochemicalsPlant ExtractsSecologanin Tryptamine AlkaloidsAntioxidantsApoptosisCell Line, TumorCell ProliferationDrug SynergismHeLa CellsHumansProto-Oncogene Proteins c-bcl-2Antineoplastic Agents, PhytogenicAntioxidantsmitragyninePhytochemicalsPlant ExtractsProto-Oncogene Proteins c-bcl-2Secologanin Tryptamine AlkaloidsAnticancer activityAntioxidant activityMitragyna speciosaMitragynineSynergistic effect

Identifiers

PMID41813913
PMCPMC13099967

What Socratic holds

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LicenceCC BY
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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.