Taraxerol Induces Cell Apoptosis through A Mitochondria-Mediated Pathway in HeLa Cells

Xiangyang Yaoi1, Binyu Lu2, Chaotian Lü1

  • 1Department of Biology and Food Engineering, Bengbu University, Bengbu, China.

Cell Journal
|August 25, 2017
PubMed
Abstract

Insights

Taraxerol induces apoptosis in cervical cancer cells by disrupting mitochondrial function and activating key cell death pathways. This natural compound shows promise as a potential anti-cervical cancer therapeutic agent.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Pharmacology

Background:

  • Taraxerol exhibits anti-cancer properties, including apoptosis induction.
  • The precise mechanisms by which taraxerol triggers apoptosis remain unclear.
  • This study investigates taraxerol's impact on the mitochondrial apoptotic pathway.

Purpose of the Study:

  • To elucidate the role of taraxerol in inducing apoptosis in HeLa cells.
  • To determine the involvement of the mitochondrial pathway, including cytochrome c release and caspase activation.
  • To explore the effects of taraxerol on key apoptotic proteins and signaling pathways.

Main Methods:

  • Cell viability assessed using MTT assay.
  • Apoptosis analyzed via DAPI staining and flow cytometry.
  • Mitochondrial membrane potential (MMP) and reactive oxygen species (ROS) measured.
  • Western blot used to evaluate apoptotic protein expression and signaling pathway modulation.

Main Results:

  • Taraxerol increased ROS levels and decreased MMP in HeLa cells.
  • Apoptosis was induced via the mitochondrial pathway, evidenced by cytochrome c release and caspase-3 activation.
  • Taraxerol modulated Bcl-2 and Bax protein levels and inhibited the PI3K/Akt pathway.

Conclusions:

  • Taraxerol effectively induces apoptosis in HeLa cells through a mitochondria-dependent mechanism.
  • These findings suggest taraxerol as a potential candidate for cervical cancer treatment.

Related Concept Videos

Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
15.7K
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
9.0K
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
8.8K
Drugs that Stabilize Microtubules01:15

Drugs that Stabilize Microtubules

Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
2.8K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
19.2K