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Articles

Lactobacillus rhamnosus R0011 Treatment Enhanced Efficacy of Capecitabine against Colon Cancer in Male Balb/c Mice

, , , , , & ORCID Icon show all
Pages 2622-2631 | Received 10 Apr 2021, Accepted 01 Dec 2021, Published online: 17 Dec 2021
 

Abstract

The microbiome of the intestinal system is well-known as a modulatory factor. Having a balanced status of microbiota could help to prevent diseases, especially cancers related to the gastrointestinal system. We investigated the effects of Lactobacillus rhamnosus (Lr) and capecitabine on tumor size and physiologic features, such as bodyweight, liver enzymes, and blood profile, in a subcutaneously induced cancer model using CT-26 murine colon carcinoma cells. We divided 48 male Balb/c inbred mice into six groups. Lr had been orally pre-inoculated to the mice for 14 day consecutively. CT-26 cells were implanted subcutaneously into the mice’s flank. Following the injection of cancer cells, Lr was inoculated to the mice three times per week for four weeks. Capecitabine was inoculated in the third week after the induction of cancer. The tumor size was significantly decreased in treated groups in comparison to the cancer group (1174.5 ± 63.8, 1119.2 ± 86.3, and 985.6 ± 48 mm3 vs. 1674.2 ± 66 mm3, P < 0.0001). Data showed that Lr and capecitabine enhanced Bax/Bcl-2 ratio and caspase-3 level compared to cancer group (p < 0.0001). White blood cells (WBCs) were significantly decreased in the capecitabine group compared to probiotic group (P < 0.05). Measurement of bodyweight, liver enzymes, and interleukin-6 (IL-6) level showed that Lr, in addition to preventive and therapeutic effects, might have protective effects against chemotherapy side effects. Preventing WBCs’ reduction, protecting mice from losing weight, induction of apoptosis, and enhancing the serum level of IL-6 indicated that Lr might be associated with better management of colorectal cancer and chemotherapy side effects.

Acknowledgments

The authors acknowledge the grant support of the Tehran University of Medical Sciences. We are grateful to Tehran University of Medical Science Pre-Clinical Core Facilities (TPCF) for Micro Positron Emission Tomography Scan and analytical support.

Authors’ Contributions

Rahimpour M and Rahimi AM performed the experiments, statistical analysis and manuscript preparation. Nabavizadeh F, and Halimi Sh, designed and organized the study. Ashabi G involved in study design and prepared the manuscript and statistical analysis. Bacterial supplementation supervised by Halimi Sh. Histological essay evaluated by Panahi M. Sample collection was also supervised by Alemrajabi M.

Ethics Approval

All procedures in this investigation were approved by the Tehran University of Medical Sciences Ethics Committee (IR.TUMS.MEDICINE.REC.1399.651) which corresponds to the national guidelines for animal care (NIH guidelines; Guide for the Care and Use of Laboratory Animals, NIH Publication 86-23).

Disclosure statement

The authors declare they have no conflict of interests.

Data Availability Statement

The data sets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Additional information

Funding

This study was supported by Tehran University of Medical Sciences Fund (grant No. 96-02-30-36852).

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