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mRNAs biomarker related to the control of proliferation and cell death in HepG2/C3A spheroid and monolayer cultures treated with piperlongumine
Biazi, Bruna Isabela; Zanetti, Thalita Alves; Marques, Lilian Areal; Baranoski, Adrivanio; Coatti, Giuliana Castello; Mantovani, Mário Sérgio.
  • Biazi, Bruna Isabela; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
  • Zanetti, Thalita Alves; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
  • Marques, Lilian Areal; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
  • Baranoski, Adrivanio; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
  • Coatti, Giuliana Castello; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
  • Mantovani, Mário Sérgio; Center of Biological Sciences. Department of General Biology. Londrina State University. Londrina. BR
Appl. cancer res ; 40: 1-13, Oct. 19, 2020. ilus
Article in English | LILACS, Inca | ID: biblio-1283485
ABSTRACT

Background:

Cell culture (spheroid and 2D monolayer cultures) is an essential tool in drug discovery. Piperlongumine (PLN), a naturally occurring alkaloid present in the long pepper (Piper longum), has been implicated in the regulation of GSTP1 activity. In vitro treatment of cancer cells with PLN increases ROS (reactive oxygen species) levels and induces cell death, but its molecular mode of action has not been entirely elucidated.

Methods:

In this study, we correlated the antiproliferative effects (2D and 3D cultures) of PLN (CAS 20069­09-4, Sigma-Aldrich) with morphological and molecular analyses in HepG2/C3A cell line. We performed assays for cytotoxicity (MTT), comet assays for genotoxicity, induction of apoptosis, analysis of the cell cycle phase, and analysis of the membrane integrity by flow cytometry. Relative expression of mRNA of genes related to proliferation, apoptosis, cell cycle control, metabolism of xenobiotics, and reticulum endoplasmic stress.

Results:

PLN reduced the cell proliferation by the cell cycle arrest in G2/M. Changes in the mRNA expression for CDKN1A (4.9x) and CCNA2 (0.5x) of cell cycle control genes were observed. Cell death occurred due to apoptosis, which may have been induced by increased expression of proapoptotic mRNAs (BAK1, 3.1x; BBC3, 2.4x), and by an increase in 9 and 3/7 active caspases. PLN induced cellular injury by ROS generation and DNA damage. DNA damage induced MDM2 signaling (3.0x) associated with the appearance of the monastral spindle in mitosis. Genes associated with ROS degradation also showed increased mRNA expression (GSR, 2.0x; SOD1, 2.1x). PLN induce endoplasmic reticulum stress with the increase in the mRNA expression of ERN1 (4.5x) and HSPA14 (2.2x). The xenobiotic metabolism showed increased mRNA expression for CYP1A2 (2.2x) and CYP3A4 (3.4x). In addition to 2D culture, PLN treatment also inhibited the growth of 3D culture (spheroids).

Conclusion:

Thus, the findings of our study show that several gene expression biomarkers (mRNAs) and monastral spindle formation indicated the many pathways of damage induced by PLN treatment that contributes to its antiproliferative effects
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: RNA, Messenger / Cell Death / Cell Culture Techniques / Cell Proliferation / Dioxolanes / Antineoplastic Agents Limits: Humans Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Center of Biological Sciences/BR

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Full text: Available Index: LILACS (Americas) Main subject: RNA, Messenger / Cell Death / Cell Culture Techniques / Cell Proliferation / Dioxolanes / Antineoplastic Agents Limits: Humans Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Center of Biological Sciences/BR