Figures
Abstract
Background
Colorectal cancer is common. Polyunsaturated fatty acids (PUFAs) exert growth-inhibitory and pro-apoptotic effects on colon cancer cells. Metabolites of PUFAs such as prostaglandins (PGs), leukotrienes (LTs) and lipoxins (LXs) play a significant role in colon cancer.
Methods
Human colon cancer LoVo and RKO cells were cultured with different concentration of PUFAs and 5-fluorouracil (5-FU) in vitro. Cell morphological changes, fatty acid composition, formation of PGE2, LTB4 and LXA4 and expression of COX-2, ALOX5, PGD synthase (PGDS), microsomal prostaglandin E synthase (mPGES) were assessed in LoVo and RKO cells when supplemented with PUFAs and 5-FU.
Results
PUFAs and 5-FU inhibited growth of LoVo and RKO cells to the same extent at the doses used and produced significant alterations in their shape. As expected, higher concentrations of supplemented PUFAs were noted in the cells compared to control. LA, GLA, AA, ALA and EPA supplementation to LoVo cells suppressed production of PGE2, LTB4,and ALOX5, mPGES expression, but enhanced that of LXA4; whereas DHA enhanced PGE2 and LXA4 synthesis but decreased LTB4 formation and COX-2, ALOX5, mPGES expression. In contrast, 5-FU enhanced formation of PGE2, LTB4 and mPGES expression, but suppressed LXA4 synthesis and COX-2 expression. PGE2, LTB4 synthesis and ALOX5 expression was suppressed by LA, GLA, ALA and DHA; whereas AA, EPA and 5-FU enhanced PGE2 but paradoxically AA decreased and EPA and 5-FU enhanced LTB4 synthesis in RKO cells. All the PUFAs tested enhanced, while 5-FU decreased LXA4 formation in RKO cells; whereas GLA, AA, and 5-FU augmented while LA, ALA, EPA and DHA enhanced COX-2 expression in RKO cells.
Citation: Zhang C, Yu H, Ni X, Shen S, Das UN (2015) Growth Inhibitory Effect of Polyunsaturated Fatty Acids (PUFAs) on Colon Cancer Cells via Their Growth Inhibitory Metabolites and Fatty Acid Composition Changes. PLoS ONE 10(4): e0123256. https://doi.org/10.1371/journal.pone.0123256
Academic Editor: Surinder K. Batra, University of Nebraska Medical Center, UNITED STATES
Received: July 29, 2014; Accepted: February 21, 2015; Published: April 17, 2015
Copyright: © 2015 Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: UND is in receipt of Ramalingaswami fellowship of the Department of Biotechnology, New Delhi during the tenure of this study. This work was supported, in part, by grants from the Department of Biotechnology (DBT No. BT/PR11627/MED/30/157/2010), Department of Science and Technology (No. IR/SO/LU/03/2008/1) under Intensification of Research in High Priority Areas (IRPHA) to UND. Author UND is the President and CEO of UND Life Sciences without any financial compensation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: UND is the President and CEO of UND Life Sciences without any financial compensation. UND Life Sciences performs research in the area of essential fatty acids and their metabolites and their role in various physiological and pathological processes. UND Life Sciences has no products in the market pertaining to the work reported in the present manuscript. Other authors have declared that no competing interests exist. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials. The specific roles of this author is articulated in the 'author contributions' section.
Introduction
Colorectal cancer is common both in males and females, with the highest incidence in Australia and New Zealand, Europe, and North America [1]. Western diet is rich in saturated fats and contains insufficient amounts of total polyunsaturated fatty acids (PUFAs) with the ratio between n-3 and n-6 being ~ 1: 20 that is considered to promote development of colorectal cancer. Previously, we and others showed that PUFAs (LA, GLA, AA, ALA, EPA and DHA) have inhibitory effect on the growth of tumor cells with little or no cytotoxic action on normal cells [2–5].
LA (linoleic acid = 9-cis,12-cis-octadecadienoic acid; 18:2 n-6) and ALA (α-linolenic acid = 9-cis,12-cis,15-cis-octadecatrienoic acid; 18:3 n-3) are essential fatty acids (EFAs) that form precursors to their respective long chain metabolites namely γ-linolenic acid (GLA; 18:3 n-6), dihomo-γ-linolenic acid (DGLA; 20:3 n-6) and arachidonic acid (AA, 20:4 n-6) and eicosapentaenoic acid (EPA, 20% n-3) and docosahexaenoic acid (DHA, 22:6 n-3) respectively. It is believed that Δ6 and Δ5 desaturases and respective elongases convert LA and ALA to their respective long-chain metabolites [6]. Tumor cells are known to be deficient in PUFAs, especially in AA, EPA and DHA due to decreased activity of enzymes Δ6 and Δ5 desaturases [7]. It may be noted that DGLA, AA and EPA form precursors to various prostaglandins (PGs), thromboxanes (TXs) and leukotrienes (LTs), whereas AA, EPA and DHA form precursors to lipoxins (LXs) (from AA), resolvins (from EPA and DHA) and protectins and maresins (from DHA) which play a significant role in inflammation and cancer [8]. In general, PGs, TXs, and LTs are pro-inflammatory in nature, produce immunosuppression and promote tumor cell proliferation. LXs, resolvins, protectins and maresins have potent anti-inflammatory actions [9, 10], but their exact role in the proliferation of tumor cells is not well documented though some studies did suggest that LXs may suppress their growth [6–8]. Although, it is believed that enhanced formation of various PGs, LTs and TXS from various PUFAs could be responsible for the cytotoxic action of PUFAs, there is no general consensus on this due to controversial results reported [6–8]. In contrast to the cytotoxic actions of PUFAs on tumor cells, some of these fatty acids, especially, GLA, PGE1 and PGI2 have been shown to possess cytoprotective and genoprotective actions [11–13]. On the other hand, overexpression of cyclooxygenase-2 (COX-2), which leads to the formation of excess of PGE2, has been associated with pro-inflammatory events and higher incidence of colorectal cancer [14–16]. These evidences indicate that COX-2 is a potential target for anti-cancer treatment. This is supported by the observation that n-3 PUFAs: DHA and EPA in combination with radiotherapy suppressed the growth of HT29 colon cancer cells that was associated with decreased COX-2 expression [17]. In addition, the microsomal PGE2 synthase (mPGES) is functionally linked to COX-2, which mediates the final regulatory step of PGE2 biosynthesis and are overexpressed in various cancers [18, 19].
In the present study, we evaluated the effect of various PUFAs (LA, GLA, AA of n-6 series and ALA, EPA, DHA of n-3 series) on the growth of colon cancer LoVo and RKO cells in vitro and compared these results with the known anti-cancer drug 5-fluorouracil (5-FU). In addition, we studied the effect of various PUFAs and 5-FU on alterations in the fatty acid composition, formation of PGE2, LTB4 and LXA4 and the expression of COX-2 that have not been reported previously.
Materials and Methods
Materials
The colorectal cancer cell lines, LoVo (undifferentiated) and RKO (semi-differentiated) were obtained from the Institute of Biochemistry and Cell Biology Shanghai Institute for Biological Sciences, Chinese Academy of Sciences. ALA, EPA, DHA, LA, GLA, AA and 5-FU were purchased from Sigma (St. Louis, MO, USA). RPMI1640 medium were purchased from GIBCO (Grand Island, NY, USA).
Cell culture
LoVo and RKO cells were cultured in RPMI Medium1640 (GIBCO) supplemented with 10% fetal bovine serum, penicillin (100 U/ml), streptomycin (100 U/ml) and grown in a 5% CO2 humidified incubator at 37°C. The stock solutions of ALA, EPA, DHA, LA, GLA, and AA were prepared as described previously [20]. However, 5-FU was dissolved in high purity water as stock solution with the concentration of 50 mM. The stock solutions of fatty acids and 5-FU were filter-sterilized and freshly diluted with cell culture media when used. In all the studies, the doses of fatty acids and 5-FU used for LoVo were as follows: 5-FU 10μM, ALA 150 μM/ml, DHA 150 μM/ml, EPA 150 μM/ml, LA 150 μM/ml, AA 150 μM/ml and GLA 300 μM/ml and the cell density used was:1×105 cells/ml; while the density of RKO was 5×104 cells/ml and the dose of 5-FU, ALA, DHA, EPA, LA, AA, and GLA used were 0.4μM, 140μM/ml, 120μM/ml, 120μM/ml, 120μM/ml, 120μM/ml, 200μM/ml respectively.
MTT assay and cell morphology determination
MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenylte-trazolium bromide (Sigma, USA)) assay was used to determine the effect of ALA, EPA, DHA, LA, GLA, AA and 5-FU on the proliferation of LoVo and RKO cells. MTT assay was performed as described previously [21].
LoVo cells were seeded in 24-well plates with a volume of 1 mL at a density of 1×105 cells/ml, while the density of RKO was 5×104 cells/ml. 24 hours after seeding, the cells were supplemented with different doses of various fatty acids and 5-FU for 48h. At the end of incubation, cell morphological changes were observed using an inverted light microscope (Nikon, Tokyo, Japan).
Fatty acid analysis of the cells
LoVo and RKO cells seeded in 50mL cell culture flasks supplemented with various PUFAs and 5-FU for 48h were then harvested using trypsin. Subsequently, cells were washed twice with PBS, resuspended in 0.5 mL high purity water. The fatty acids were esterified as recommended by Seppänen-Laakso T [22], and Cellular content of fatty acids was measured by gas chromatography as described in detail previously [20]. The peaks were identified by comparing the retention times with known methyl ester standards (FAME Mix, Supelco) and the fatty acids were quantified by an external standard method.
LTB4, PGE2 and LXA4 measurement
For the determination of LTB4, PGE2, and LXA4 levels in LoVo and RKO culture medium, cells were seeded in a 6-well plate for overnight and treated with pre-determined doses of PUFAs and 5-FU for 48h. At the end of the treatment period, the medium was harvested by centrifuging at 2,000×g for 5 min to remove floating cells. Subsequently, the supernatant was collected and assayed using LTB4, PGE2, and LXA4 ELISA kits following the manufacturer’s instructions (WESTANG Bio-TECH, Shanghai, China). The results were corrected by the protein level before expressing as percentage of the control.
Determination of COX-2 and ALOX5 activity
LoVo and RKO cells were cultured in 6-well plates and treated with various PUFAs and 5-FU for 48h, at the end of which the cultural supernatant collected by centrifuging at 2,000×g for 5 min were used for COX-2 and ALOX5 levels analysis by competitive enzyme-linked immunosorbent assay (ELISA) purchased from Xitang (Shanghai, China) and CUSABIO (Wuhan, China), respectively. The results were corrected by the protein level before expressing the values as percentage of the control.
mRNA analysis
Total RNA was extracted from cultured LoVo and RKO cells supplemented with various PUFAs and 5-FU for 48h with 500μL TRIzol reagent (Haogene Biotech, Hangzhou, China). cDNA was synthesized by a reverse transcription reaction with 1st-Strand cDNA Synthesis Kit (Haogene Biotech, Hangzhou, China) from 500ng of total RNA according to the manufacturer’s instructions. Real-time quantitative PCR (RT-PCR) was performed using Power SYBR Master Mix (Invitrogen). For each reaction, 12.5 ul of Power SYBR Master Mix, 0.5μl of each PCR primer, 1μl of DNA template, 10.5μl of distilled water were added. Human18S rRNA was chosen as a reference for gene expression analysis, and further analysed according to the 2－ΔΔCT method.
Primers (Sangon Biotech) used were: Human 18s (F; GACTCAACACGGG-AAACCTCAC, R; CCAGACAAATCGCTCCACCAAC), Human PGDS (F; CCTGCCCCAAACCGATAAGTG, R; GCTCGGGGAAGGAACAGAGCAG), Human mPGES (F; CCCCAGTATTGCAGGAGCGAC, R; GCATCCAGGCGACA-AAAGGGTTAG).
Results
PUFAs induced morphological changes in LoVo and RKO cells
The morphological changes of LoVo and RKO cells in response to different doses of PUFAs and 5-FU treatment were analyzed under light microscopy and the results are shown in Figs 1 and 2. The results showed that untreated cells grew well with a normal shape, which could be found by their uniform distribution with intensive connections and confluence. However, compared with the control group, PUFAs and 5-FU treatment of LoVo and RKO cells decreased their number, and cell shape was distorted with rounding up, which suggests that PUFAs and 5-FU inhibited the proliferation of these cells.
Effect of PUFAs on the fatty acids composition of colon cancer cells
In the present study, we analyzed fatty acid composition of LoVo and RKO cells in response to supplementation with various PUFAs and 5-FU for 48h and are shown in Table 1 and Figs 3 and 4. The ratio of unsaturated fatty acids/saturated fatty acids (S/U) and the ratio of n-6 PUFAs/n-3 PUFAs (n-6/n-3) were also calculated. These results indicated that when supplemented with PUFAs, fatty acid profiles of LoVo and RKO cells were significantly different compared with control group. As shown in Table 1, it is noteworthy that levels of supplemented fatty acids were significantly increased in LoVo and RKO cells. For instance, LoVo cells supplemented with ALA, DHA, EPA, LA, AA, GLA showed a 54.9-fold, 12.32-fold, 16.6-fold, 13.95-fold, 3.17-fold and 39.88-fold higher concentrations respectively compared to the control. On the other hand, RKO cells treated with ALA, DHA, EPA, LA, AA, GLA showed a 14.09-fold, 54.81-fold, 225.95-fold, 31.71-fold, 44.46-fold and 18.41-fold increase in the concentrations of these fatty acids respectively. It is noteworthy that both in LoVo and RKO cells showed a substantial increase in EPA and DHA levels when supplemented with EPA suggesting that EPA is converted to its long-chain metabolite DHA. In addition, supplementation of AA enhanced the content of AA and EPA in both LoVo and RKO cells. Surprisingly, LoVo cells supplemented with GLA resulted in not only a significant increase in their GLA content but also an increase in ALA, EPA, DHA, LA and AA. In contrast, RKO cells supplemented with GLA showed a decrease in ALA, EPA, DHA and LA content in comparison to control.
While assessing the ratio between unsaturated fatty acids/saturated fatty acids (U/S), it was noted that both LoVo and RKO cells showed a higher ratio of U/S in all PUFAs treatments compared to the control as is evident form the results shown in Table 1 and Figs 3 and 4. LoVo cells supplemented with n-6 PUFAs (LA, AA and GLA) resulted in a 17.52, 10.09 and 29.68% increases for the sum of n-6 PUFAs and 1.13, 0.1, 1.46% decreases for the sum of n-3 PUFAs compared to control. Similarly, supplementation with n-3 PUFAs (ALA, DHA and EPA) to LoVo cells resulted in a 34.52, 17.22, 16.83% increases in the total amount of n-3 PUFAs and 14.78, 14.73, 12.12% decreases for the sum of n-6 PUFAs in comparison with control. RKO cells that were supplemented with LA, AA and GLA showed a 30.69, 53.33 and 35.84% increase in the concentrations of n-6 PUFAs compared to the control respectively. On the other hand, RKO cells that were supplemented with ALA, DHA and EPA showed an increase in the levels of these n-3 fatty acids by 49.21, 35.83 and 15.18% respectively compared to the control.
Supplementation of 5-FU to LoVo and RKO cells produced far few changes in the composition of n-6 PUFAs and n-3 PUFAs in comparison with control. On the other hand, LoVo cells showed a significant increase in the content n-9 PUFAs and decreased content of saturated fatty acids. In contrast, supplementation of 5FU produced a significant increase in the saturated fatty acid content and a significant decrease in its n-9 PUFAs in RKO cells.
Effects of PUFAs on the PGE2, LTB4 and LXA4 level
PGE2 and LTB4 have been shown to posses pro-inflammatory actions, promote tumor cell invasion, enhance their metastasis, upregulate VEGF expression, inhibit tumor cell apoptosis and suppress immune function [13, 23]. Thus, both PGE2 and LTB4 may act as anti-apoptotic molecules and enhance tumor growth. In contrast, lipoxin A4 is a potent anti-inflammatory molecule and opposes the actions of PGE2 and thus, could suppress tumor cell proliferation, invasiveness and metastasis [13]. In view of this, we determined the secretion of PGE2, LTB4 and LXA4 by LoVo and RKO cells following supplementation with various PUFAs and 5-FU for 48 hours.
As is evident from these results shown in Fig 5, PGE2 secretion by LoVo cells when supplemented with LA, GLA, AA, ALA, EPA and 5-FU was suppressed, while DHA enhanced its secretion compared with the control. On the other hand, LA, GLA, AA, ALA, EPA and DHA (all PUFAs tested) decreased LTB4 secretion to a significant degree by LoVo cells while 5-FU enhanced the same. Results shown in Fig 6 revealed that RKO cells supplemented with LA, GLA, DHA and ALA produced decreased amounts of PGE2, while AA, EPA and 5-FU induced a substantial increase in its production. In contrast, RKO cells showed decreased production of LTB4 when supplemented with LA, GLA, AA, ALA and DHA and showed increased production in response to EPA and 5-FU challenge.
Values in the same column with different letters are significantly different (p<0.05).
Values in the same column with different letters are significantly different (p<0.05).
In comparison to these results, all PUFAs tested enhanced the production of LXA4 by LoVo and RKO cells while, 5-FU treatment inhibited LXA4 secretion in both these cells as shown in Figs 6 and 7.
Values in the same column with different letters are significantly different (p<0.05).
Effects of PUFAs on the expression of COX-2 and ALOX5
COX-2 plays an important role in both inflammation and colon carcinogenesis and hence, it has been suggested that agents that suppress its expression may be useful in inhibiting these two processes [24]. On the other hand, growing body of evidence indicates that arachidonate 5-lipoxygenase (ALOX5) is a crucial regulator of inflammation and cancer pathogenesis [25]. In the present study, we measured the expression of COX-2 following supplementation of PUFAs and 5-FU, which showed that, in general, PUFAs (except for AA on LoVo and GLA and AA on RKO cells) down-regulated the expression of COX-2 compared to control as is evident from the results shown in Figs 6 and 7, while PUFAs (except for EPA on RKO cells) down-regulated the expression of ALOX5 compared to control as seen from the results depicted in Figs 7 and 8. On the other hand, 5-FU inhibited the expression of COX-2 and ALOX5 in LoVo cells but enhanced in RKO cells.
Values in the same column with different letters are significantly different (p<0.05).
Effects of PUFAs on the expression of PGDS and mPGES
Microsomal prostaglandin E synthase (mPGES) and PGD synthase (PGDS) mediate the final regulatory step of PGE2 and prostaglandin D2 biosynthesis respectively and have been implicated in tumor pathogenesis [26, 27]. Hence, we investigated the expression of PGE synthase and PGD synthase using real-time PCR following supplementation of PUFAs and 5-FU. Results of this study shown in Table 2 indicated that PGE2 synthase expression in LoVo was increased compared to the control group, while PUFAs (except for EPA and GLA on LoVo) up-regulated the expression of PGD synthase compared to control. Additionally, neither the expression of PGE2 synthase nor PGD synthase was detected in RKO cells because of their low expression in these cells.
Discussion
There is evidence to suggest that PUFAs, especially, EPA and DHA have anti-cancer activity both in vitro and in vivo. Previously, we reported that PUFAs have substantial cytotoxic action on tumor cells by enhancing free radical generation, lipid peroxidation, altering membrane composition and inducing mitochondrial dysfunction [2, 3, 20, 28]. In an extension of this study, we now evaluated whether supplementation of PUFAs could produce changes in the formation of their metabolites that may have a role in bringing about their growth inhibitory action. The changes in the morphological appearance, fatty acid composition, PGE2, LTB4 and LXA4 secretion and COX-2, ALOX5, mPGES, PGDS expression noted in LoVo and RKO cells in response to supplementation of different PUFAs indicates that there could occur substantial changes in the way these fatty acids are metabolized by cancer cells that could account for their tumoricidal action. It is noteworthy that semi-differentiated colon cancer RKO cells are more sensitive to the actions of PUFAs and 5-FU than undifferentiated colon LoVo cancer cells.
Tumor cells are known to be deficient in the activity of Δ6 and Δ5 desaturases [29, 30] and thus, may contain substantially lower amounts of GLA, AA, EPA and DHA compared to normal cells. The exact reason for the low activity of desaturases in cancer cells is not known. Since PUFAs can undergo peroxidation easily and generate free radicals that are toxic to cells [2, 3], it is likely decreased activity of desaturases is a defence mechanism adopted by tumor cells to protect themselves from these toxic molecules. As expected, supplemented fatty acids suppressed the proliferation of LoVo and RKO cells due to their incorporation in to the cell membrane to a significant degree. But, what is surprising is the observation that supplementation of AA enhanced EPA content to a significant degree both in LoVo and RKO cells suggesting that a close interaction exists between n-3 and n-6 fatty acids [9, 20]. Previously, none described the existence of such an interaction between n-3 and n-6 PUFAs influencing the formation of PGs, LTs, and other metabolites. In fact, previous studies showed that supplementation of EPA and DHA decreased AA content in the cell membrane lipid pool of tumor cells [14–16, 23].
AA, EPA and DHA form precursors not only to pro-inflammatory molecules PGs, TXs and LTs but also give rise to potent anti-inflammatory molecules LXs, resolvins, protectins, maresins and nitrolipids [9, 31, 32]. PGE2 and PGF2α and LTA4 and LTB4 are known to be produced in significantly higher amounts by tumor cells, which may enhance their motility and invasive capacity [33]. In contrast, LXA4 may promote apoptosis and inhibit growth of tumors by suppressing tumor angiogenesis by inhibiting the production of VEGF [34]. This suggests that balance between pro-inflammatory PGs, LTs and TXs and anti-inflammatory LXs, resolvins, protectins, maresins and nitrolipids (that are formed due to reaction between various PUFAs and nitric oxide and these compounds have anti-inflammatory actions) may determine the degree of proliferation and invasive capacity of tumor cells [8]. In addition, PGD2 can also inhibit cell proliferation and induce apoptosis in various cell types, including colon cancer cells [35]. In the present study, the expression of PGD synthase (a rate limiting enzyme that regulates the synthesis of prostaglandin D2) was found to be up-regulated by PUFAs (except for EPA and GLA) compared to control in LoVo. On the other hand, it was observed that majority of the PUFAs except DHA inhibited the release of PGE2, while all PUFAs inhibited LTB4 production but enhanced the synthesis and release of LXA4 in LoVo cells. Similarly, all PUFAs except AA and EPA inhibited PGE2 and LTB4 (except EPA) but enhanced the production of LXA4 in RKO cells (see Figs 5 and 6). Furthermore, it is noteworthy that DHA, EPA and AA induced significant increase in the secretion of LXA4 compared to other PUFAs suggesting that anticancer actions of these three PUFAs may due to their ability to enhance the formation of LXA4 in addition to suppressing PGE2 and LTB4 synthesis. This is evident from the data shown in Fig 9 wherein we calculated the PGE2/LXA4 ratio. All PUFAs reduced this ratio in LoVo cells compared to control except 5-FU, whereas AA, EPA (AA > EPA) and 5-FU increased this ratio in RKO cells. Thus, in general, all PUFAs enhanced the formation of LXA4 and decreased the synthesis of PGE2 and LTB4 tilting the balance more towards anti-inflammatory status. (Fig 9: Effect of ALA, DHA, EPA, LA, AA, GLA and 5-FU on the expression of PGE2/LXA4 in LoVo and RKO cells in vitro; Values in the same column with different letters are significantly different (p<0.05). A summary of the data obtained in the present study showing the changes that occurred as a result of the action of various PUFAs and 5-FU on the secretion of PGE2, LTB4, LXA4, ALOX5, COX-2, PGDS and mPGES activity in LoVo and RKO is given in Table 3 for easy reference. (Table 3: Summary of the effect of various PUFAs and 5-FU on the secretion of PGE2, LTB4, LXA4, ALOX5, COX-2, PGDS and mPGES activity in LoVo and RKO cells in vitro. N/D = Below detectable limits).
Values in the same column with different letters are significantly different (p<0.05).
COX-2 is needed for the synthesis of PGs, LTs, TXs and LXs. Several studies reported that COX-2 expression is elevated in colorectal tumors in comparison to normal colorectal tissue [36]. Our results reported here indicated that all PUFAs except AA (in LoVo) and GLA and AA (in RKO) suppressed the expression of COX-2. This is consistent with the results that PGE2 and LTB4 secretion is inhibited by these PUFAs that may, in turn, inhibit tumor cell proliferation. It may be mentioned here that COX-2 is also needed for the synthesis of LXA4 that may explain why AA enhanced its (COX-2) activity in LoVo and RKO cells that corresponded to the enhanced production of LXA4 seen in these cells. It is noteworthy that the secretion of PGE2 and LTB4 corresponded with the activity of mPGES and ALOX5, which indicates that upregulated activity of mPGES and ALOX5 could be responsible for the enhanced secretion of PGE2 and LTB4 seen in the LoVo and RKO cells.
For the first time, we showed that the growth inhibitory action of PUFAs is due to an increase in the production of LXA4 in colon cancer cells. Previously, several studies showed that EPA and DHA suppress the proliferation of tumor cells by inhibiting the expression of COX-2. In contrast to these studies, we noted in the present study that AA suppressed the growth of colon cancer cells and at the same time upregulated that of COX-2 expression yet enhanced the production of LXA4 that explains its growth suppressive action. Hence, we suggest that decrease in the production of PGE2, leukotriene B4 and an increase in LXA4 is more crucial for the growth inhibitory actions of PUFAs rather than suppression of COX-2.
It is noteworthy that though all the PUFAs tested and 5-FU induced same degree of growth inhibition of both LoVo and RKO cells, changes observed in the secretion of PGE2, LTB4 and LXA4 and COX-2 expression were found to be variable. Despite this, certain generalizations are possible. Low amounts of AA, EPA and DHA in tumor cells, due to decreased activity of Δ6 and Δ5 desaturases, may trigger to augment PGE2 synthesis as a compensatory mechanism [37]. This is supported by the observation that plasma and/or other body fluid PGE2 levels are increased in inflammatory conditions lupus, rheumatoid arthritis and multiple sclerosis [38–40] (and cancer is also an inflammatory condition) in which deficiency of PUFAs has been described [41, 42]. On the other hand, oral administration of AA and DHA to animals with inflammatory colitis showed enhanced LXA4 synthesis with little or no change in PGE2 formation in AA supplemented animals while DHA decreased PGE2 formation with no change in LXA4 [43]. These results suggest that when AA, EPA and DHA levels are low, administration of these fatty acids augments the production of LXA4 (and possibly that of other anti-inflammatory molecules such as resolvins, protectins and maresins) with marginal changes in PGE2 synthesis. In addition, LXA4 is known to suppress PGE2 synthesis [44, 45]. It is likely that enhanced LXA4 production outweighs the changes in PGE2 levels such that ultimately inflammatory process is suppressed. Since LXA4 inhibited the growth of LoVo and RKO tumor cells [29, 46], enhanced the production of LXA4 on supplementation of AA, EPA and DHA and other PUFAs, it is likely that augmented formation of LXA4 (in addition to decreased formation of PGE2 and LTB4) could be responsible for the decreased growth of LoVo and RKO cells noted in the present study.
In conclusion, our findings indicate that PUFAs induce toxicity at 48h of colon cancer LoVo and RKO cells in vitro. Cytotoxic action of PUFAs may be associated with decrease in the production of pro-inflammatory PGE2 and LTB4, COX-2, mPGES and ALOX5 expression and enhanced formation of anti-inflammatory LXA4 (Table 2). These results are supported by our recent data that showed that lipoxins, resolvins and protectins have a direct growth inhibitory action on tumor cells [45, 46]. One important question that arises when only in vitro studies are performed is how relevant are these test tube results in an in vivo situation. Previously, we did perform both in vivo experiments and limited clinical studies that did show that some of these PUFAs, especially GLA, have tumoricidal actions against a variety of tumors [47–50]. Given the tumoricidal action of various PUFAs, it is important to dissect the mechanisms of their action. Since such studies are not always possible in an in vivo situation and humans, we have resorted to the present study to know the metabolism of PUFAs and the expression of mPGES, COX-2 and ALOX5 are altered in colon cancer cells. It is also true that all tumor cells many not behave in the same fashion (colon cancer cells may metabolize PUFAs differently compared to neuroblastoma cells) and the metabolism of different PUFAs may be different among several tumor cells. Nevertheless some generalizations may be possible. Thus, based on the results of the present study and our previous studies, we propose that tumor cell growth inhibitory or cytotoxic action of PUFAs is likely to be associated with decrease in the production of pro-inflammatory PGE2 and LTB4, COX-2, mPGES and ALOX5 expression and enhanced formation of anti-inflammatory lipoxins, resolvins and protectins. Further studies are being performed to verify these possibilities.
Author Contributions
Conceived and designed the experiments: SS UND. Performed the experiments: CZ HY XN. Analyzed the data: SS UND. Contributed reagents/materials/analysis tools: SS UND. Wrote the paper: SS UND.
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