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May 9, 2026Current Gastroenterology Reports0 citationsOpen Access

Fermented Durian Tempoyak as a Source of Probiotics for Colorectal Cancer Prevention through Gut Microbiome Modulation

WNWing Soon NgNNNancy Choon‐Si NgRWR S Y Wong

Key Points

  • To explore the role of fermented durian tempoyak as a dietary source of probiotics in preventing colorectal cancer through gut microbiome modulation.
  • Examined fermented durian tempoyak's probiotic strains, such as Lactiplantibacillus plantarum, in relation to colorectal cancer prevention.
  • Discussed mechanisms including modulation of inflammatory pathways and gut barrier integrity related to dysbiosis.
  • Highlighted the need for strain characterization and standardized human trials in high-risk populations.
  • Probiotic strains in tempoyak may reduce tumor burden in colorectal cancer models.
  • LAB strains can attenuate inflammatory pathways such as NF-κB, MAPK, and COX-2.
  • Evidence supports tempoyak as a plausible agent for microbiome-based colorectal cancer chemoprevention.

Abstract

PURPOSE OF REVIEW: Colorectal cancer (CRC) remains a major global and Malaysian public health concern, with increasing recognition of gut dysbiosis as a contributor to colorectal tumorigenesis. This review examines fermented durian tempoyak as a culturally relevant, probiotic-rich traditional food with potential application in CRC prevention through gut microbiome modulation. RECENT FINDINGS: Dysbiosis may promote CRC through disruption of gut barrier integrity, chronic mucosal inflammation, immune dysregulation, reactive oxygen species (ROS)-mediated DNA damage, and altered microbial metabolism leading to carcinogenic metabolites such as secondary bile acids and hydrogen sulphide. Tempoyak commonly contains lactic acid bacteria, particularly Lactiplantibacillus plantarum, as well as Limosilactobacillus fermentum and Levilactobacillus brevis. Preclinical evidence suggests that related LAB strains can attenuate NF-κB, MAPK, STAT3, IL-17, and COX-2-associated inflammatory pathways, reduce immune-cell infiltration and oxidative stress, restore mucus and tight junction proteins, modulate bile acid metabolism, and reduce tumor burden in CRC or colitis-associated CRC models. Current evidence supports the mechanistic plausibility of tempoyak-associated LABs as microbiome-based agents for CRC chemoprevention. However, direct evidence using tempoyak-derived strains remains limited, and translation is constrained by strain-specific effects, microbial variability, sensory acceptability, safety and standardisation issues, and uncertain LAB viability after cooking. Future studies should prioritise strain characterisation, starter culture standardisation, probiotic stabilisation strategies, CRC-specific preclinical models, and well-designed human trials in high-risk populations.

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Cite This Study

Ng et al. (2026) studied this question.

synapsesocial.com/papers/69fed021b9154b0b8287725ahttps://doi.org/10.1007/s11894-026-01043-4
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