Chemical Characterization and Cytotoxic Activity of Antarctic Macroalgae Extracts against Colorectal Cancer

Background/Aim: Antarctic seaweeds are considered a promising source of compounds with anticancer activity. Colorectal cancer (CRC) is one of the most incident cancers with high mortality rates worldwide. This work aimed to characterize chemically extracts of the Antarctic macroalgae Iridaea cordata, Cystosphaera jacquinotii and Desmarestia anceps and to evaluate the cytotoxic effects against human colon cancer HCT 116 cell line. Materials and Methods: The extracts were obtained by depletion using an ultrasound probe and were identified by High-Performance Liquid Chromatography (HPLC) and Gas Chromatography coupled with Mass Spectrometry (GC-MS). Cell viability by MTT assay. Results: Hexanic and chloroform extracts of the I. cordata and the hexanic, chloroform and methanolic extracts of D. were able to inhibit growth of colorectal cancer cells in the incubation (24, and 72 h). Through analysis, 01 were in and 02 compounds in the chloroform I. The of D. macroalgae extract to Carotenoid analysis in sion: Extracts of macroalgae I. Cordata and D. anceps may be a source of therapeutic agents against CRC. Carotenoids Profile: Two peaks were identified in the chromatogram of the red algae I. cordata: zeaxanthin and β-carotene. For brown seaweed D. anceps, four peaks were indetified: fucoxanthin, violaxanthin, zeaxanthin and β-carotene fucoxanthin. For brown algae C. jacquinotii, three peaks were identified: fucoxanthin, violaxanthin and β-carotene.


Introduction
Colorectal cancer (CRC) prevalence is one of the major public health problems worldwide due to its high incidence and mortality. CRC is the third most common cancer among men, and the second among women, accounting for about 1.4 million new cases and almost 700 thousand deaths in 2012 [1]. The most recent estimate of Brazilian National Cancer Institute [2] for 2018/2019 is that CRC will affect 17,380 men and 18,890 women, consisting of the third and second causes of cancer deaths respectively. CRC incidence distribution varies across Brazil's regions. A high incidence is reported in the most developed economically and industrialized regions, such as Southeast and South. These may be correlated with a western way of life as obesity, smoking, sedentary lifestyle, high consumption of red meat and processed foods, low vegetable intake, and aging of the population, similar to developed countries [2] [3]. Regardless the advances in therapeutic interventions over the last decades, mortality rates caused by CRC remain around 40%, mainly due to liver metastases in advanced stages of the disease [4]. Therefore, research on new natural compounds with anticancer properties and reduced side effects have become important in providing alternatives for the CRC treatment [5].
The oceans cover more than 70% of the earth's surface and contain an extraordinary diversity of life, with an enormous resource for potential therapeutic agents. Algae are adapted to a hostile environment, developing secondary metabolites as a defense and adaptation strategies. The anticancer potential activity of many compounds extracted from macroalgae, which provides important chemical scaffolds for the discovery of new drugs for the management of CRC has been recently reported [6] [7]. Previous studies have shown that algae-extracted compounds, such as fucoxanthin and sulfated polysaccharides (fucoidan), have antitumor activity against colorectal cancer cell lines. In addition, fucoidan had a protective effect against chemotherapy toxicity when used concomitantly with colorectal cancer therapy [8] [9]. Fucoidan reduced fatigue, allowing patients to have extended treatment time, which is crucial for chemotherapy effectiveness [10].
Among the thousands of macroalgae species, Antarctic seaweeds survive in one of the most hostile environment in the planet, being exposed to solar radiation in the summer, low luminosity and photosynthetic activity in the winter, ice melting and herbivory. Because they have adapted to the polar environment, these algae may be considered a promising source of new bioactive compounds, including those with anticancer activity [7]. Therefore, the objective of this study was to chemically characterize different extracts obtained from Antarctic seaweeds and to evaluate the antitumor activity of these extracts in order to isolate new molecules with potential anticancer activity in the future.

Materials and Methods
Seaweed Sample and Preparation of Extracts: The red seaweed Iridaea cordata (Turner) Bory de Saint-Vincent and brown seaweeds Cystosphaera jacquinotii (Montagne) Skottsberg and Desmaretia anceps Montagne were collected during the Brazilian Antarctic Operation XXXIII (Table 1). Macroalgae fixed to the substrate were collected from the intertidal region during periods of low tide. The seaweeds were washed with seawater to remove epiphytes and frozen at −20˚C. Species identification and the classification were performed according to specimen morphology [11] and deposited in the Herbarium of Botanical Institute of São Paulo (SP), Brazil. The frash seaweeds were lyophilized and tritured with liquid nitrogen to obtain a uniform sample. The extracts were obtained by depletion, in which 10 g of each algal sample was sequentially soaked with 50 mL of hexane, chloroform and methanol, using ultrasound probe (VC 750, Sonics and Materials Inc., Newtown, USA) at a constant frequency of 20 kHz and 20% amplitude for 30 minutes. The temperature was monitored and did not exceed 18˚C. The extration was repeated three times. After, the extracts were vacuum filtered through 0.45 µm membrane and the solvent was rotoevaporated (Büchi R-300 Labortechnik AG, Flawil, Switzerland). Three extracts (hexane, choroform and methanol) were obtained for each algae.
Chemical Analysis of Extracts by Gas Chromatography Coupled with Mass (GC-MS): The extracts were analyzed by GC-MS (QP2010, Shimadzu, Kyoto, Japan) with a 30 m fused silica capillary column (HP-5MS with 0.25 μm film, Agilent). A sample (1 μL) was injected at temperature of 220˚C and with split of 1:10. Helium was used as the carrier gas at a flow rate of 1 mL·min −1 with the following temperature ramp: initial temperature of 60˚C with a of 5˚C per min ramp up to 260˚C, which was maintained for 10 min. Peak identification of crude algal extracts was performed based on comparing the obtained mass spectra with those available in NIST 08 and Wiley 9 libraries.
Carotenoids Analysis: The analysis of the carotenoids profile of the macroalgae was determined as described in literature [13]. Briefly, chromatographic separations were carried out by High-Performance Liquid Chromatography (HPLC, Shimadzu system) equipped with two LC-10AD pumps, a SIL-10ADVP automatic

Discussion
Colorectal carcinoma has become a worldwide public health problem due to its high incidence and mortality. This type of cancer is the third most prevalent and represents the largest cause of non-smoking cancer deaths. The increase in incidence in recent years in developing countries such as Brazil has been observed [14].
Despite advances in diagnosis and treatment, mortality rates remain high due to the lack of government investments to create programs for the early detection of disease in developing countries, such as Brazil, and intrinsic characteristics such as tumor resistance to conventional chemotherapy and side effects. Due to these factors, the search for new compounds with anticancer activity is of extreme importance [15].
Natural compounds play a very important role in the discovery of new drugs with antitumor activity. In the last three decades, the discovery of secondary metabolites with biological activity from macroalgae has grown substantially, however, of approximately 25,000 species of algae described, only 15 are used biotechnologically on a large scale [16]. Antarctic algae are adapted to one of the most adverse conditions on the planet, such as the polar environment, may be a promising source of compounds with anticancer activity.
The present study analyzed the cytotoxicity of extacts of Antarctic macroalgae I. cordata, D. anceps and C. jacquinotti and found that hexanic and chloroform extracts of I. cordata and hexane, chloroform and methanolic extracts of D. anceps seaweeds were cytotoxic against the HCT 116 cell line after 24, 48 and 72 h exposition in a dose-dependent manner (p < 0.05). GC-MS analysis shows the presence of cholest-5-en-3ß-ol (epicholesterol) and octadecanoic acid in I. cordata extracts. Epicholeterol is an epimeric form of cholesterol present in menbranes cell and is related to cell permeability and membrane movement [20]. Octadecanoic acid or stearic acid is a fatty acid, a unique long-chain satured fatty acid (SFA), the only one that is not correlated with the risk of cardiovascular diseases, being a candidate for use in the food industry [21]. In the spectrum of D. anceps, peaks corresponding to compounds with described biological activity were identified, such as hexadecanoic acid, phytol and fucosterol. Hexadecanoic acid is a saturated fatty acid with anti-inflammatory activity [22]. Phytol, open chain diterpene, is with antimycobacterium activity [23]. Fucosterol, a sterol typically found in brown algae and has been attributed to it several biological activities, such as anti-inflammatory, anti-oxidant, hepatoprotective and anticancer (against HL 60 cell line) [24].
HPLC-carotenoids analysis allowed to identify the presence of four compunds β-carotene, fucoxanthin, zeaxanthin and violaxanthin. Carotenoids have many functions in the human body, including antioxidant activity (β-carotene), retinal protective effect against solar radiation damage (zeaxanthin) and reduction of serum triglyceride levels (astaxanthin) [25]. Fucoxanthin is a colored marine carotenoid present in microalgae and brown algae. Many studies have reported the anticancer activity of fucoxanthin and its derivative fucoxanthinol against several types of tumor cell lines, including colorectal carcinoma [8] [26].
Also, fucoxanthin is related to decrease of risk factors for cardiac diseases, such as obesity, diabetes, high blood pressure, chronic inflammation, plasma and hepatic triglyceride, and cholesterol concentrations and antioxidant activity. Fucoxanthin, violaxanthin and β-carotene had a photoprotective effect [26] [27].
Many studies have reported on the anticancer activity of extracts and compounds isolated from macroalgae against colorectal cancer strains, but the biological structure/activity relationship needs to be elucidated [8] [9] [10]. The present study suggests that the hexanic and chloroform extracts of I. cordata and the hexanic, chloroform and methanolic extracts of D. anceps are promising candidates for investigations, including the development of drugs to combat colorectal cancer.

Conclusion
The hexanic and chloroform extracts of the red seaweed I. cordata and the hexanic, chloroform and methanolic extracts of brown seaweed D. anceps inhibited the growth of the HCT 116 cell line, suggesting that these algae are a promising source of bioactive compounds with anticancer properties. Further studies to isolate and elucidate the bioactive compounds present in these extracts are required.