4.4 Article

Alteration of nanomechanical properties of pancreatic cancer cells through anticancer drug treatment revealed by atomic force microscopy

Journal

BEILSTEIN JOURNAL OF NANOTECHNOLOGY
Volume 12, Issue -, Pages 1372-1379

Publisher

BEILSTEIN-INSTITUT
DOI: 10.3762/bjnano.12.101

Keywords

anticancer drug; atomic force microscopy; nanomechanical properties; pancreatic cancer cells

Funding

  1. Natural Science Foundation of Hebei Province [C2021202002]
  2. National Key R&D program of China [2020YFC1107403]
  3. National Natural Science Foundation of China [31600753]

Ask authors/readers for more resources

The mechanical properties of normal pancreatic cells were found to be greater than those of pancreatic cancer cells, with different cancer cell lines exhibiting varying levels of Young's modulus. Additionally, treatment with doxorubicin hydrochloride resulted in changes in the mechanical properties of cancer cells.
The mechanical properties of cells are key to the regulation of cell activity, and hence to the health level of organisms. Here, the morphology and mechanical properties of normal pancreatic cells (HDPE6-C7) and pancreatic cancer cells (AsPC-1, MIA PaCa-2, BxPC-3) were studied by atomic force microscopy. In addition, the mechanical properties of MIA PaCa-2 after treatment with different concentrations of doxorubicin hydrochloride (DOX) were also investigated. The results show the Young's modulus of normal cells is greater than that of three kinds of cancer cells. The Young's modulus of more aggressive cancer cell AsPC-1 is smaller than that of less aggressive cancer cell BxPC-3. In addition, the Young's modulus of MIA PaCa-2 rises with the increasing of DOX concentration. This study may provide a new strategy of detecting cancer, and evaluate the possible interaction of drugs on cells.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available