AI Article Synopsis

  • This study aimed to investigate how the SNC19/ST14 gene affects the behavior of colorectal cancer cells after being introduced into them.
  • The gene was successfully inserted into RKO colorectal cancer cells using a specific vector, and various methods were employed to analyze cell characteristics such as growth, adhesion, and cytoskeletal changes.
  • Results showed that while SNC19/ST14 altered the organization of F-actin and reduced cell adherence to the extracellular matrix, it did not significantly change the cell cycle, apoptosis, or overall cell proliferation, except at high expression levels.

Article Abstract

Objective: To study the effect of SNC19/ST14 gene transfection and expression into colorectal cancer cells on biological behavior.

Methods: The recombination vector pSecTag2a-SNC19/ST14 was constructed, and transfected into the RKO colorectal cancer cell line by liposome. The transfected cell was screened by real time PCR, Western Blot and Immunohistochemical technique. The population doubling time (T(D)) and cell cycle of the transfected cell were analyzed by MTT assay and flow cytometer. Rhodamine-labeled Phallodin was used to label the cell cytoskeletal protein-F-actin, and the F-actin distribution was observed by confocal scanning microscope. The adhesion ability of the transfected cell to extracellular matrix (ECM) was measured by MTT assay.

Results: The full length Open Reading Frame (ORF) of SNC19/ST14 gene was inserted into the vector pSecTag2a, and transfected into RKO cells, and expressed successfully. The changes of F-actin organization took place in transfected cell. The Adherence ability of the transfected cell to ECM was decreased, but the proliferation ability was not significantly changed except highly expressing of the SNC19/ST14, and not the cell cycle and the apoptosis.

Conclusion: SNC19/ST14 gene was successfully expressed into the RKO cell line, and could influence on the cell cytoskeletal protein (F-actin) organization and on cell adherence ability to ECM, but could not make the cell cycle, apoptosis and proliferation ability change significantly.

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