# The synergistic tumor growth-inhibitory effect of probiotic Lactobacillus on transgenic mouse model of pancreatic cancer treated with gemcitabine

**Authors:** Shan-Ming Chen, Wee-Wei Chieng, Szu-Wei Huang, Li-Jin Hsu, Ming-Shiou Jan

PMC · DOI: 10.1038/s41598-020-77322-5 · Scientific Reports · 2020-11-23

## TL;DR

This study shows that combining probiotics with chemotherapy can reduce pancreatic cancer progression and improve treatment tolerance in mice.

## Contribution

The study demonstrates the synergistic effect of probiotics and gemcitabine in a transgenic mouse model of pancreatic cancer.

## Key findings

- Combined gemcitabine and probiotics reduced PanIN formation and expression of vimentin and Ki-67.
- Probiotics lowered AST and ALT levels, indicating reduced liver damage in treated mice.
- High-dose probiotics alone also inhibited PanIN changes and liver enzyme elevation.

## Abstract

Pancreatic cancer is one of the most lethal and chemo-resistant cancers worldwide. Growing evidence supports the theory that the gut microbiota plays an essential role in modulating the host response to anti-cancer therapy. The present study aimed to explore the effect of probiotics as an adjuvant during chemotherapy for pancreatic cancer. An LSL-KrasG12D/−-Pdx-1-Cre mouse model of pancreatic ductal adenocarcinoma (PDAC) was created to study the effects of using four-week multi-strain probiotics (Lactobacillus paracasei GMNL-133 and Lactobacillus reuteri GMNL-89) as an adjuvant therapy for controlling cancer progression. At 12 weeks of age, pancreatitis was induced in the mice by two intraperitoneal injection with caerulein (25 μg/kg 2 days apart). Over the next 4 weeks the mice were treated with intraperitoneal injections of gemcitabine in combination with the oral administration of probiotics. The pancreas was then harvested for analysis. Following caerulein treatment, the pancreases of the LSL-KrasG12D/−-Pdx-1-Cre transgenic mice exhibited more extensive pancreatic intraepithelial neoplasia (PanIN) formation. Combined treatment with gemcitabine and probiotics revealed a lower grade of PanIN formation and a decrease in the expression of vimentin and Ki-67. Mice that received gemcitabine in combination with probiotics had lower aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Notably, the use of high-dose probiotics alone without gemcitabine also had an inhibitory effect on PanIN changes and serum liver enzyme elevation. These findings suggest that probiotics are able to make standard chemotherapy more effective and could help improve the patient’s tolerance of chemotherapy.

## Linked entities

- **Genes:** PDX1 (pancreatic and duodenal homeobox 1) [NCBI Gene 3651]
- **Proteins:** PRELID1 (PRELI domain containing 1), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Chemicals:** gemcitabine (PubChem CID 60750), caerulein (PubChem CID 16129675), alanine aminotransferase (PubChem CID 251717)
- **Diseases:** pancreatic cancer (MONDO:0005192), pancreatitis (MONDO:0004982)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, SMAD4 (SMAD family member 4) [NCBI Gene 4089] {aka DPC4, JIP, MADH4, MYHRS}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, Pdx1 (pancreatic and duodenal homeobox 1) [NCBI Gene 18609] {aka IDX-1, IPF-1, Ipf1, Mody4, STF-1, pdx-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, PDX1 (pancreatic and duodenal homeobox 1) [NCBI Gene 3651] {aka GSF, IDX-1, IPF1, IUF1, MODY4, PAGEN1}, Slc17a5 (solute carrier family 17 (anion/sugar transporter), member 5) [NCBI Gene 235504] {aka 4631416G20Rik, 4732491M05, AST, ISSD, NSD, SD}, Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, VIM (vimentin) [NCBI Gene 7431], Kras (Kras proto-oncogene, GTPase) [NCBI Gene 16653] {aka K-Ras, K-Ras 2, K-ras, Ki-ras, Kras-2, Kras2}, IL27 (interleukin 27) [NCBI Gene 246778] {aka IL-27, IL-27A, IL27A, IL27p28, IL30, p28}, Vim (vimentin) [NCBI Gene 22352], Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}
- **Diseases:** necrosis (MESH:D009336), rheumatoid arthritis (MESH:D001172), PanIN (MESH:D002578), fibrosis (MESH:D005355), skin rash (MESH:D005076), KC (MESH:D010195), asthma (MESH:D001249), systemic lupus erythematosus (MESH:D008180), non-small cell lung cancer (MESH:D002289), cancer metastasis (MESH:D009369), diabetes (MESH:D003920), deaths (MESH:D003643), breast cancer (MESH:D001943), thrombocytopenia (MESH:D013921), liver cancer (MESH:D006528), multiple sclerosis (MESH:D009103), gastrointestinal neoplasms (MESH:D005770), inflammatory cytokines (MESH:D000080424), abnormalities in liver function (MESH:D056486), colonic cancer (MESH:D015179), inflammation (MESH:D007249), intestinal damage (MESH:D007410), gastric cancer (MESH:D013274), fever (MESH:D005334), PDAC (MESH:D021441), ulcerative colitis (MESH:D003093), obesity (MESH:D009765), dysbiosis (MESH:D064806), carcinogenesis (MESH:D063646), Pancreatic cancer (MESH:D010190), flu-like syndromes (MESH:D007251), metastasis (MESH:D009362), ischemia-reperfusion damage (MESH:D015427), alcohol abuse (MESH:D000437), bone marrow suppression (MESH:D001855), bladder cancer (MESH:D001749), chronic pancreatitis (MESH:D050500), carcinogenic (MESH:D011230), thrombocytosis (MESH:D013922), liver (MESH:D017093), H&amp;E (MESH:D016751), Th2-driven diseases (MESH:D004194), autoimmune diseases (MESH:D001327),  (MESH:D004195)
- **Chemicals:** urea nitrogen (MESH:C530477), water (MESH:D014867), nucleoside (MESH:D009705), gemcitabine triphosphate (MESH:C533693), H&amp;E (MESH:D006371), PBS (MESH:D007854), Cae + Prob (-), Prob (MESH:D011339), Glucose (MESH:D005947), Cae (MESH:D002108), ethanol (MESH:D000431), Cr (MESH:D002857), 2', 2'-difluorodeoxycytidine (MESH:D000093542), cholecystokinin (MESH:D002766), short chain fatty acids (MESH:D005232), paraffin (MESH:D010232), amines (MESH:D000588), creatinine (MESH:D003404),  (MESH:D000964),  (MESH:D003841)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Lacticaseibacillus paracasei (species) [taxon 1597], Mus musculus (house mouse, species) [taxon 10090], Pelodryas caerulea (green tree frog, species) [taxon 30344], Lactobacillus (genus) [taxon 1578]
- **Cell lines:** LSL — Homo sapiens (Human), Hemophilia A, Induced pluripotent stem cell (CVCL_A4EK), KC — Homo sapiens (Human), Amelanotic melanoma, Cancer cell line (CVCL_UD29), /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985), GMNL133 — Mus musculus (Mouse), Hybridoma (CVCL_J918)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC7683550/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC7683550/full.md

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Source: https://tomesphere.com/paper/PMC7683550