Related Experiment Video
Updated: Nov 10, 2025

10:23
Evaluation of Caspase Activation to Assess Innate Immune Cell Death
Published on: January 20, 2023
3.5K
LOSS OF CAS3 AND INCREASE OF BAX EXPRESSION ASSOCIATED WITH PROGRESSION OF CERVICAL INTRAEPITHELIAL NEOPLASIA.
G Pkhakadze1, Z Bokhua1, T Asatiani1
1Tbilisi State Medical University, Georgia.
Georgian Medical News
|April 5, 2021
Summary
Apoptosis markers Cas3 and Bax, along with proliferation marker Ki67, are significantly altered during cervical intraepithelial neoplasia (CIN) progression. These changes indicate potential biomarkers for monitoring cervical cancer development.
Area of Science:
- Oncology
- Cell Biology
Background:
- Apoptosis is crucial in human cancer development, including cervical carcinoma.
- Cervical intraepithelial neoplasia (CIN) represents a spectrum of pre-cancerous changes in the cervix.
Purpose of the Study:
- To analyze the expression of Caspase-3 (Cas3) and Bax proteins.
- To correlate Cas3 and Bax expression with proliferation index (Ki67) and Estrogen Receptor (ER) status.
- To investigate these markers during the progression of cervical intraepithelial neoplasia (CIN).
Main Methods:
- Studied 140 cervical specimens, categorized by co-infection status.
- Employed standard immunohistochemistry to detect Ki67, Cas3, Bax, and ER.
- Analyzed protein expression correlations with CIN progression.
Main Results:
- Cas3 expression decreased, while Bax expression increased with CIN progression.
- Bax expression negatively correlated with Cas3 and ER expression.
- Bax expression positively correlated with Ki67 expression.
Conclusions:
- Deregulation of apoptosis (increased Bax, decreased Cas3) and increased proliferation (Ki67) are linked to CIN progression.
- These protein expressions may serve as valuable biomarkers for CIN progression and cervical cancer development.
Related Concept Videos
Caspases
13.0K
Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside...
13.0K
The Intrinsic Apoptotic Pathway
7.3K
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...
7.3K
The Extrinsic Apoptotic Pathway
7.1K
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...
7.1K

