Research Papers:

Intratumoral heterogeneity of the therapeutical response to gemcitabine and metformin

Dietmar Zechner _, Florian Bürtin, Ann-Christin Albert, Xianbin Zhang, Simone Kumstel, Maria Schönrogge, Josefine Graffunder, Hao-Yu Shih, Sarah Müller, Tobias Radecke, Robert Jaster and Brigitte Vollmar

PDF  |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2016; 7:56395-56407. https://doi.org/10.18632/oncotarget.10892

Metrics: PDF 2134 views  |   HTML 2909 views  |   ?  


Dietmar Zechner1,*, Florian Bürtin1,*, Ann-Christin Albert1, Xianbin Zhang1, Simone Kumstel1, Maria Schönrogge1, Josefine Graffunder1, Hao-Yu Shih1, Sarah Müller2, Tobias Radecke1, Robert Jaster2, Brigitte Vollmar1

1Institute for Experimental Surgery, Rostock University Medical Center, 18057 Rostock, Germany

2Division of Gastroenterology, Department of Medicine II, Rostock University Medical Center, 18057 Rostock, Germany

*These authors contributed equally to this work

Correspondence to:

Dietmar Zechner, email: [email protected]

Keywords: pancreatic adenocarcinoma, chemotherapy, syngeneic orthotopic cancer model, microenvironment, pH Blot

Received: January 18, 2016     Accepted: July 18, 2016     Published: July 28, 2016


Cancer heterogeneity and microenvironmental aspects within a tumor are considered key factors influencing resistance of carcinoma cells to distinct chemotherapeutical agents. We evaluated a high concentration of metformin in combination with gemcitabine on a syngeneic orthotopic mouse model using 6606PDA cells. We observed reduced tumor size and reduced cancer cell proliferation after three weeks of chemotherapy with either compound and noticed an additive effect between gemcitabine and metformin on tumor weight. Interestingly, distinct areas of the carcinoma responded differently to either compound. Metformin inhibited the proliferation of cancer cells close to the desmoplastic reaction, whereas gemcitabine inhibited the proliferation of cancer cells mainly 360–570 μm distant to the desmoplastic reaction. Indeed, co-culture of pancreatic stellate cells with 6606PDA, 7265PDA or MIA PaCa-2 cells increased gemcitabine resistance. Metformin resistance, however, was increased by high glucose concentration in the medium. Other factors such as hypoxia or the pH of the medium had no influence on gemcitabine or metformin induced inhibition of cancer cell proliferation. These data demonstrate a spatial heterogeneity in drug resistance within pancreatic adenocarcinomas and that microenvironmental aspects such as supply of glucose and the presence of pancreatic stellate cells regulate cancer cell sensitivity towards metformin or gemcitabine.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 10892