In vitro anticancer activity of fucoidan extracted from Sargassum cinereum against Caco-2 cells

S Sivasankara Narayani1, S Saravanan2, J Ravindran3

  • 1Department of Microbiology, Ayya Nadar Janaki Ammal College, Sivakasi, India.

Insights

Fucoidan from brown seaweed shows anti-cancer effects against colon cancer cells. It induces apoptosis and increases reactive oxygen species (ROS) production, suggesting therapeutic potential.

Area of Science:

  • Marine Biology
  • Biochemistry
  • Cancer Research

Background:

  • Fucoidan, a sulfated polysaccharide from brown seaweed, exhibits diverse bioactivities, including anti-cancer properties.
  • The precise mechanisms of fucoidan's anti-cancer and apoptotic effects on colon cancer cells require further investigation.

Purpose of the Study:

  • To evaluate the anti-cancer and apoptotic activity of fucoidan from Sargassum cinereum against the Caco-2 colon cancer cell line.
  • To elucidate the underlying mechanisms, including cytotoxicity, apoptosis induction, and reactive oxygen species (ROS) generation.

Main Methods:

  • Cytotoxicity assays were performed to determine the inhibitory concentration (IC50).
  • Apoptosis was assessed using AO/EB, Hoechst, and Annexin V/PI staining.
  • Mitochondrial membrane potential and ROS production were measured via flow cytometry.

Main Results:

  • Fucoidan demonstrated dose-dependent inhibition of Caco-2 cell growth, with an IC50 of 250 μg/ml.
  • Apoptosis induction was confirmed through morphological changes and specific staining techniques.
  • Fucoidan significantly increased ROS production and mitochondrial membrane permeability.

Conclusions:

  • Fucoidan from Sargassum cinereum exerts significant anti-cancer and apoptotic effects on Caco-2 colon cancer cells.
  • The anti-cancer mechanism involves the enhancement of ROS production.
  • Fucoidan holds promise as a potential therapeutic agent for various cancer types.

Related Concept Videos

ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH301:11

orthopara-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3

All ortho–para directors, excluding halogens, are activating groups. These groups donate electrons to the ring, making the ring carbons electron-rich. Consequently, the reactivity of the aromatic ring towards electrophilic substitution increases. For instance, the nitration of anisole is about 10,000 times faster than the nitration of benzene. The electron-donating effect of the methoxy group in anisole activates the ortho and para positions on the ring and stabilizes the corresponding...
7.3K
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
16.1K
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H01:13

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
6.6K
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
14.8K
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
5.4K
Extraction: Effects of pH00:53

Extraction: Effects of pH

Consider a neutral form of an amine, B, with a partition coefficient, K, in a liquid mixture containing organic and aqueous phases. The pH of the aqueous phase affects the charge on acidic and basic solutes, and the charged form is usually more soluble in the aqueous phase. Suppose the conjugate acid form of the amine is soluble only in the aqueous phase while the base form is soluble in both phases. Then the distribution coefficient, D, can be given as the ratio of amine concentration in the...
1.3K