Anticancer activity of Caesalpinia sappan by downregulating mitochondrial genes in A549 lung cancer cell line

F1000Res. 2022 Feb 11:11:169. doi: 10.12688/f1000research.76187.2. eCollection 2022.

Abstract

Background: The standardization and mechanism of action of Caesalpinia sappan as an anticancer agent are still lacking. This study aimed to understand the mechanism of action of C,sappan extract as an anticancer agent. Methods: This study was conducted using the A549 lung cancer cell line to understand the mechanism of action of C. sappan extract as an anticancer agent. The cytotoxicity activity, cell cycle progression, apoptosis, protein-related apoptosis (i.e., BCL-2and BAX protein) assays, and RNA sequencing were performed level were measured. Moreover, the antioxidant activity, total flavonoids, and phenolics of C.sappan were also assessed. Results: C.sappan has strong antioxidant activity (22.14 ± 0.93 ppm) total flavonoid content of (529.3 ± 4.56 mgQE/g), and phenolics content of (923.37 ± 5 mgGAE/g). The C.sappan ethanol extract inhibited cancer cell growth and arrested at G0/G1 phase of cell cycle, inducing apoptosis by increasing BAX/BCL-2 protein ratio in A549 lung cancer cell line. Furthermore, results from RNA sequencing analysis showed that C.sappan ethanol extract caused downregulation of genes acting on mitochondrial function including adenosine triphosphate (ATP) production and respiration. Conclusions: This study demonstrated that C.sappan has the ability to inhibit cancer cell growth by inducing apoptosis and mitochondrial dysfunction in A549 cells.

Keywords: A549 cells; ATP production; Caesalpinia sappan; apoptosis; cytotoxicity; mitochondrial dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Adenosine Triphosphate
  • Antineoplastic Agents* / pharmacology
  • Antioxidants / pharmacology
  • Caesalpinia*
  • Ethanol
  • Flavonoids / pharmacology
  • Genes, Mitochondrial
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Plant Extracts / pharmacology
  • bcl-2-Associated X Protein / genetics

Substances

  • Antineoplastic Agents
  • Antioxidants
  • Flavonoids
  • Plant Extracts
  • bcl-2-Associated X Protein
  • Ethanol
  • Adenosine Triphosphate

Grants and funding

This work was supported by the Directorate General Higher Education, Ministry of Research and Technology Republic of Indonesia, via a World Class Research grant assigned to Widodo, Yoga Dwi Jatmiko, and Masruri (grant number: 023/E4.1/AK.04.PT/2021).