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Applied Biological Chemistry
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Cow milk derived-fat inhibits the proliferation of liver cancer-cells

Applied Biological Chemistry volume 67, Article number: 7 (2024) Cite this article

Abstract

Cow milk is a widely consumed liquid diet, and its fatty acid composition impacts its nutritional and biochemical properties. However, research on the anticancer efficacy of cow milk-derived fat in liver cancer cells is limited. This study investigated the antiproliferative and apoptotic effects of cow milk-derived fat in human hepatoma HepG2 cells. Additionally, the effects of cow milk-derived fat on cell cycle progression and Janus kinase (JAK)-2/signal transducer and activator of transcription (STAT)-3 signaling in HepG2 cells were assessed. Furthermore, the histone deacetylase inhibitory and 2,2-diphenyl-1-picrylhydrazyl radical scavenging potential of cow milk-derived fat were examined. The results demonstrate that cow milk-derived fat can exert antiproliferative and anticlonogenic effects and induce apoptosis in HepG2 cells dose-dependently. Furthermore, cow milk-derived fat induced cell cycle arrest, suppressed the levels of pJAK-2 and pSTAT-3, and inhibited the total histone deacetylase activity in HepG2 cells. The fatty acid profile of cow milk-derived fat revealed that palmitic, oleic, and linoleic acids were abundant as saturated, monounsaturated, and polyunsaturated fatty acids, respectively. Our findings provide a new scientific basis for the development of anticancer strategies that utilize cow milk-derived fat and its derivatives against liver cancer.

Introduction

According to the Food and Agriculture Organization, cow milk and its products are the most commonly consumed forms of mammalian milk, accounting for nearly 81.26% of global milk production [1]. The consumption of cow milk has several health benefits, including bone strengthening, blood pressure reduction, and reducing the risk of some chronic diseases owing to its antimicrobial and antioxidant properties [2]. It is a good source of proteins, water-soluble vitamins (riboflavin and B12), fat-soluble vitamins (A and E), fat, and minerals, such as calcium, phosphorus, sodium, magnesium, potassium, and iodine [3]. Cow milk-derived fat contains more than 400 types of fatty acids, and it is present mainly as fat globules [4]. Although season, breed, climate, health, diet, and lactation stage can affect the fatty acid composition of cow milk, palmitic acid (16:0) is the most abundant saturated fatty acid, followed by stearic acid (18:0) and myristic acid (14:0) [5, 6]. Among the unsaturated fatty acids, oleic acid (18:1) is the most abundant, followed by linoleic (18:2) and α-linoleic (18:3) acids. In addition, cow milk contains odd-chain fatty acids produced by the cow’s ruminal bacteria [4, 7].

The anticancer effects of odd-chain amino acids have gained considerable attention in fatty acid biochemistry. Heptadecanoic acid (C17:0) exerts anticancer effects on non-small cell lung carcinoma cells [8]. Moreover, pentadecanoic acid (C15:0) has been shown to have anti-cancerous effects on breast cancer stem cells [9]. Valeric acid also exerts anticancer effects on liver cancer cells [10]. Notably, when breast cancer stem-like cells were exposed to a combination of pentadecanoic acid and tamoxifen, the cells re-expressed estrogen receptor-α [11]. A recent study identified a series of odd-chain fatty acids as novel inhibitors of histone deacetylase (HDAC) 6. These play a key role in tumorigenesis through histone deacetylation, thereby contributing to tumor cell survival and proliferation. This further strengthens the biochemical significance of fatty acids [12]. Several investigations have shown the anticancer properties of specific fatty acids [13,14,15,16,17,18,19,20]. However, research on the anticancer efficacy of cow milk-derived fat, which contains a diverse range of fatty acids, including high concentrations of saturated fatty acids, is very limited in liver cancer models.

The liver plays a major role in fatty acid metabolism. Fatty acids accumulate in the liver through uptake from the bloodstream and de novo biosynthesis [21]. Dietary fat is an important source of hepatic fatty acids. Following consumption, fats are hydrolyzed in the intestinal lumen. Once absorbed into the intestine, free fatty acids are reassembled into triglycerides, which are packaged into chylomicrons and transported to the muscle and adipose tissue. In hepatocytes, the remaining triglycerides found in remnants of the chylomicrons are then transported to the liver, where they undergo intracellular processing to release free fatty acids [21]. Liver cancer is a major global health concern. Current treatment modalities include radiotherapy, chemotherapy, surgery, and immunotherapy, alone or in combination. However, these methods have limitations that can reduce their effectiveness, highlighting the need for innovations in the treatment of liver cancer [22].

The Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway is an essential signal transduction mechanism that controls gene expression and cellular functioning in the presence of growth factors and cytokines, such as epidermal growth factor (EGF) family members, interferons, and interleukins [23]. Upon ligand-induced activation, JAKs phosphorylate the cytoplasmic portion of receptor tyrosine kinases, creating binding sites for STATs. After binding, JAKs phosphorylate STATs. JAK-2 is one of four members of the JAK family, while STAT-3 is one of seven members of the STAT-3 family in humans [23, 24]. The JAK/STAT pathway is one of the most frequently dysregulated signaling pathways in cancer, specifically in hepatocellular carcinoma. STAT-3 is a transcription factor that is constantly activated in up to 60% of liver cancer cases [25]. The activation of STAT-3 (functioning as a transcription factor) results in the expression of multiple genes that significantly contribute to the diverse characteristics of cancer. This emphasizes the crucial involvement of STAT-3 in the development of liver cancer [25, 26].

Given that the liver plays a crucial role in metabolizing and accumulating fatty acids and that cow milk is a rich source of fatty acids, we conducted this study to explore the potential anticancer properties of cow milk-derived fat on liver cancer cells in vitro.

Materials and methods

Cell culture

The human liver cancer cells (HepG2) used in the present investigation were purchased from the American Type Culture Collection (Rockville, MD, USA) and cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Catalog number 11,965, Life Technologies Corporation, Grand Island, NY, USA) according to the supplier’s recommendations. The medium has increased nutrient concentration, particularly glucose (4.5 g/L d-Glucose), providing energy for cell metabolism. DMEM also includes a mixture of amino acids essential for protein synthesis, and it is supplemented with a broader range of vitamins and minerals necessary for cellular processes.

Cow milk sample collection

Fresh cow milk samples were purchased from a village farmer who sells cow milk for household uses in the Colombo District, Sri Lanka. According to the farmer, the samples are from a healthy, local breed (Batu cattle) who allowed to graze on natural pastures or cultivated forages and milk for this study was obtained from local cows that were milked twice a day and in the early stage of lactation. Given that Sri Lanka does not experience significant seasonal changes, the influence of seasons was not a factor considered in this study. The samples were carefully transported to the laboratory in sealed containers and used for fat extraction upon arrival at the laboratory.

Fat extraction from cow milk

Fat was extracted from cow milk samples using the Folch method with slight modifications [27]. First, 50 mL cow milk was combined with 60 mL chloroform and methanol at a 2:1 ratio (v/v) and vigorously mixed for 10–15 s. Subsequently, 10 mL water was introduced, mixed thoroughly, and left for 48 h to separate the organic and aqueous layers. The organic layer was transferred to a clean beaker, evaporated, and used for bioassays following the preparation of the stock solutions.

Cell viability assay

HepG2 cells were seeded in 96-well plates at a density of 5000 cells/well. After 24 h, the cells were treated with cow milk-derived fat (0, 0.5, 1, 1.5, 2, or 2.5 mg/mL) dissolved in dimethyl sulfoxide. The 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay and its calculations were conducted according to our previous study [12].

2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay

The DPPH radical scavenging assay and its data analysis were conducted as previously described with minor modifications [28]. Cow milk-derived fat with concentrations of 5, 10, and 20 mg/mL (dissolved in dimethyl sulfoxide) was used for the assay with catechin as the positive control.

Cell cycle analysis

Flow cytometry was used to analyze the effects of cow milk-derived fat on the liver cancer cell cycle. BD FACSDiva™ Software (BD Biosciences, NJ, USA) was employed to conduct the flow cytometric analysis. Before the analysis, HepG2 cells (3 × 104 cells) were washed with phosphate-buffered saline and then fixed using 70% ethanol for 30 min at 37 °C. Then, the cells were treated with RNase A (25 ng/mL) and stained with propidium iodide (40 µg/mL) before the analysis.

HDAC inhibitory assay

The HDAC colorimetric activity assay kit (ab1432; Abcam, MA, USA) evaluates the activity of HDACs through a colorimetric method. The experiment followed the manufacturer’s protocol provided with the kit. The concentrations of the final cow milk-derived fat samples ranged from 1 to 4 mg/mL. Absorbance was measured at 405 nm using a microplate reader. Trichostatin A was used as a positive control. The results were expressed as the percentage of enzyme activity for each sample tested compared to the untreated controls.

Colony formation assay

HepG2 cells were seeded at a density of 400 cells/dish in 60 cm-diameter cell culture dishes and incubated for 24 h. The cells were then treated with different concentrations of cow milk-derived fat for 21 days, after which the colony formation assay was conducted according to our previous studies [12].

Analysis of free fatty acids

The fatty acid compositions in the extracted fat fractions of cow milk samples were analyzed using the Association of Official Analytical Collaboration (AOAC) 996.06 method [29]. The relative peak area percentage (peak area relative to the total peak area %) was calculated following the established standards set by the AOAC protocols to express the fatty acid composition.

Western blot

Western blotting was performed as previously described [12]. All primary antibodies, except the anti-β-Actin primary antibody (approximately 1:10000 dilution), were diluted 1:1000 in skim milk. The primary antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA). Anti-rabbit immunoglobulin G secondary antibody (Vector Laboratories, Burlingame, CA, USA) was diluted to 1:5000 before use. The bands were visualized using the BS ECL Plus Kit (Biosesang, Seongnam, South Korea). Protein bands were quantified using ImageJ software (US National Institutes of Health, Bethesda, MD, USA).

Statistical analysis

Statistical analyses entailed one-way analyses of variance using GraphPad Prism software (version 7.0; GraphPad, USA). Statistical significance was considered when p < 0.05 and indicated by an asterisk (*). All experiments were performed in triplicate, and the results are presented as the mean ± standard deviation.

Results and discussion

Free fatty acid profile of cow milk-derived fat

Analysis of the fatty acid profiles revealed varying degrees of saturated, mono-, and poly-unsaturated fatty acids in cow milk-derived fat (Fig. 1). Palmitic acid (C16:0) is cow milk’s most abundant saturated fatty acid. Among monounsaturated fatty acids, oleic acid (C18:1) is the most abundant in cow milk-derived fat. Among the polyunsaturated fatty acids, linoleic acid (C18:2), is the most abundant. Pentadecylic (or pentadecanoic) acid (C15:0) and margaric (or heptadecanoic) acid (C17:0) were detected in cow milk-derived fat samples. Our findings corroborate those of previous reports highlighting the fatty acid profiles of cow milk-derived fat [4, 6, 7].

Fig. 1
figure 1

Fatty acid profile of cow milk-derived fat analyzed using the Association of Official Analytical Collaboration 996.06 method. Peak areas relative to the total peak area are shown as percentages

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Cow milk-derived fat inhibits the proliferation and colony formation ability of liver cancer cells

Cancer cells are characterized by uncontrolled proliferation. Several studies have shown that natural and synthetic compounds can inhibit cancer cell proliferation in vitro and in vivo [9, 30, 31]. Following exposure to cow-milk fat, dose- and time-dependent inhibition of cell viability was observed with IC50 values 1.501 ± 0.053 mg/mL and 1.299 ± 0.046 mg/mL for 24 and 48 h, respectively (Fig. 2A). The colony formation assay revealed that cow milk significantly inhibited colony formation in HepG2 cells (Fig. 2B, C). Cow milk contains various components with potential anticancer effects. These components include fatty acids, ceramides, sphingosines, and specific proteins [32,33,34]. Fatty acids such as trans-10, cis-12-conjugated linoleic acid [13], propionic acid [14], butyric acid [14], linoleic acid [15], elaidic acid [16], oleic acid [17], γ-linolenic acid and dihomo-γ-linolenic acid [18], palmitic acid [19], and docosahexaenoic acid [20] have been reported to exert anticancer effects on a range of human cancer cell lines. Additionally, certain odd-chain fatty acids found in cow milk, such as C15:0 and C17:0, have been shown to inhibit cancer cell growth [8, 9], suggesting that the collective presence of these antiproliferative components in cow milk may result in synergistic effects against cancer cell proliferation. In addition to cow milk, camel colostrum exosomes exert antiproliferative effects on liver cancer cell lines HepaRG [35].

Fig. 2
figure 2

Inhibitory effects of cow milk-derived fat in HepG2 cells. A A 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide assay was used to assess the antiproliferative effects of cow milk-derived fat following 24 and 48 h incubations. B Effects of cow milk-derived fat on the clonogenic ability of HepG2 cells following 21 days exposure. C Statistical quantification of colonies. We tested for statistical significance using one-way analyses of variance with Dunnett’s post hoc tests. ****p < 0.0001

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Cow milk-derived fat induces apoptosis in liver cancer cells

Cancer cells undergo apoptosis, characterized by specific morphological and biochemical changes. The activation of caspases plays a vital role in apoptosis. Specifically, caspase 3, an effector caspase, becomes active as apoptosis is initiated, promoting the transmission of apoptotic signals via poly ADP-ribose polymerase (PARP). Caspase 3 catalyzes the cleavage of PARP [36]. Hoechst 33,342 staining was employed to determine whether cow milk-derived fat mediates cytotoxic effects by inducing apoptosis. Chromatin condensation, a biochemical characteristic of apoptosis [37], was observed in HepG2 cells exposed to cow-milk fat (Fig. 3A). Western blotting results indicated that the cleaved form of caspase-3 was present in HepG2 cells exposed to cow milk-derived fat at the first two doses tested (Fig. 3B). Additionally, cow milk-derived fat significantly increased the levels of cleaved PARP in HepG2 cells (Fig. 3B). As shown in Fig. 3C, treatment with cow milk-derived fat caused a substantial increase in the sub-G1 population, from 6.78 ± 2.50% (0 mM) to 37.66 ± 3.92% (1.5 mM), indicating a potential cell cycle arrest in HepG2 cells exposed to cow-milk fat. Collectively, these findings suggest that cow milk-derived fat induces apoptosis and cell cycle arrest in HepG2 cells. Notably, a previous study reported that cow milk-derived fat enhances the effects of paclitaxel in vivo [38]. Furthermore, a recent study revealed that β-Casomorphin, a degradation product of β-casein, inhibits the metastasis of colorectal cancer [39]. Another recent study demonstrated that donkey milk induces apoptosis in triple-negative breast cancer cells [40], highlighting the apoptotic potential of milk. However, it is necessary to indicate that the consumption of dietary fat is associated with an increased risk of breast cancer [41].

Fig. 3
figure 3

Apoptotic potential of cow milk-derived fat and its effects on HepG2 cell cycle. A Hoechst 33,342 staining of HepG2 cells. Red arrows indicate condensed chromatin in Hoechst 33,342 stained HepG2 cells. B Western blot experiments showing the expression of apoptosis-associated proteins in HepG2 cells exposed to cow milk-derived fat for 24 h. Statistical quantification of C Cleaved-caspase 3 (C-Caspase 3)/parent caspase 3 and D Cleaved-poly ADP-ribose polymerase (C-PARP)/parent PARP. E Effects of cow milk-derived fat on the cell cycle of HepG2 cells. We tested for statistical significance using one-way analyses of variance with Dunnett’s post hoc tests (*p < 0.05 and **p < 0.01)

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Total HDAC inhibition by cow milk-derived fat

HDAC inhibitors are a class of small molecules that can inhibit HDAC activity, resulting in cell cycle arrest, cell growth inhibition, and apoptosis in cancer cells [42]. We previously reported that fatty acids can inhibit HDAC6 expression [12]. In addition, we repurposed bempedoic acid, a United States Food and Drug Administration (FDA)-approved ATP citrate lyase inhibitor that mimics the structure of a dicarboxylic fatty acid, as an HDAC6 inhibitor [43]. These findings have generated interest in exploring the overall HDAC-inhibitory effects of fats extracted from cow milk. As shown in Fig. 4, cow milk-derived fat inhibited HDAC activity in a dose-dependent manner, highlighting the HDAC-inhibitory potential of cow milk-derived fat.

Fig. 4
figure 4

Total histone deacetylases (HDAC) inhibitory potential of cow-milk fat. We tested for statistical significance using a one-way analysis of variance and Dunnett’s post hoc test (**p < 0.01, and ***p < 0.001)

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Cow milk-derived fat exerts antioxidant effects

The interest in antioxidants is growing rapidly, primarily because of their potential to combat the harmful effects of free radicals in the human body [44]. Several natural and synthetic compounds have been identified as free radical scavengers [44]. The results of the DPPH assay in this study indicated that cow milk-derived fat can scavenge DPPH free radicals in a dose-dependent manner with an EC50 value of 18.83 ± 1.27 (mg/mL) (Fig. 5). In addition to fatty acids, amino acids, milk-derived proteins, and minerals have been reported to contribute to the antioxidant activities of cow milk and its products [45,46,47].

Fig. 5
figure 5

The DPPH radical scavenging ability of cow-milk fat. We tested for statistical significance using a one-way analysis of variance and Dunnett’s post hoc test (****p < 0.0001)

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Cow milk derived-fat suppresses the JAK-2/STAT-3 signaling in HepG2 cells

We recently reported that pentadecanoic acid can effectively suppress JAK-2/STAT-3 signaling in breast cancer stem cells [9]. This finding prompted us to investigate the potential of fatty acids as potent JAK-2/STAT-3 inhibitors. It motivated us to examine various food sources rich in fatty acids to identify natural inhibitors of JAK-2/STAT-3 signaling. We observed a significant decrease in the level of pSTAT-3/STAT-3 (Fig. 6A) and, although not statistically significant, a decrease in the level of pJAK-2/JAK-2 (Fig. 6B) in HepG2 cells when exposed to cow milk-derived fat at the tested dose of 1.5 mg/mL (Fig. 6A and B). This dose is close to the IC50 value obtained from the anti-proliferative assay after 24 h of exposure. These findings indicate that cow milk-derived fat has the potential to inhibit the proliferation of HepG2 cells, possibly by modulating the JAK-2/STAT-3 signaling pathway in liver cancer cells. It has been reported that silencing or inhibiting STAT-3 can induce apoptosis in vitro and in vivo [48,49,50]. In addition, STAT-3 has been reported to participate in cell proliferation, metastasis, and epithelial-mesenchymal transition (EMT) in liver cells, suggesting its pivotal oncogenic role in liver cancer cells [51, 52].

Fig. 6
figure 6

Western blot analysis showing the expression of signal transducers and activators of transcription Janus kinase (JAK)-2, pJAK-2 and signal tranducer and activator of transcription (STAT)-3, and pSTAT-3 in HepG2 cells exposed to cow milk-derived fat for 24 h. Statistical quantification of A pSTAT-3/STAT-3 and B pJAK-2/JAK-2. p represents phosphorylated forms. We tested for statistical significance using one-way analyses of variance with Dunnett’s post hoc tests (***p < 0.001)

Full size image

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Abbreviations

AOAC:

Association of Official Analytical Collaboration

DPPH:

2,2-Diphenyl-1-picryhydrazyl

EGF:

Epidermal growth factor

FDA:

The United States Food and Drug Administration

HDAC:

Histone deacetylase

JAK:

Janus kinase

MTT:

3-(4,5-Dimethylthiazol- 2-yl)-2,5-diphenyltetrazolium bromide

PARP:

Poly ADP-ribose polymerase

STAT:

Signal transducer and activator of transcription

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Acknowledgements

We would like to thank Editage (www.editage.co.kr) for English language editing.

Funding

The present study was supported by grants from the UNESCO-TWAS and the Swedish International Development Cooperation Agency (Grant number 22–140 RG/BIO/AS_I) and by Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Education (2016R1A6A1A03012862).

Author information

Author notes

  1. Meran Keshawa Ediriweera and Do Manh Cuong contributed equally to this work.

Authors and Affiliations

  1. Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Colombo, No. 25, Kynsey Road, Colombo 8, Sri Lanka

    Meran Keshawa Ediriweera

  2. Interdisciplinary Graduate Program in Advanced Convergence Technology and Science, Jeju National University, Jeju, 63243, Republic of Korea

    Do Manh Cuong & Somi Kim Cho

  3. Subtropical, Tropical Organism Gene Bank, Jeju National University, Jeju, 63243, Republic of Korea

    Somi Kim Cho

  4. Department of Biotechnology, College of Applied Life Sciences, SARI, SARI, Jeju National University, Jeju, 63243, Republic of Korea

    Somi Kim Cho

Authors
  1. Meran Keshawa Ediriweera
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  2. Do Manh Cuong
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  3. Somi Kim Cho
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Contributions

MKE, DMC and SKC designed the study. MKE and DMC performed the experiments, analyzed the data and wrote the manuscript. MKE, DMC and SKC confirm the authenticity of all the raw data.

Corresponding author

Correspondence to Somi Kim Cho.

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Ediriweera, M.K., Cuong, D.M. & Cho, S.K. Cow milk derived-fat inhibits the proliferation of liver cancer-cells. Appl Biol Chem 67, 7 (2024). https://doi.org/10.1186/s13765-024-00860-3

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