Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2017  |  Volume : 13  |  Issue : 52  |  Page : 595--599

Anti-cancer effects of polyphenolic compounds in epidermal growth factor receptor tyrosine kinase inhibitor-resistant non-small cell lung cancer


Hyungmin Jeong1, Ai N. H. Phan2, Jong-Whan Choi3,  
1 Wonju High School, Yonsei University, Wonju, Gangwon-Do, Republic of Korea
2 Department of Biochemistry; Department of Global Medical Science, Institute of Lifestyle Medicine, Nuclear Receptor Research Consortium, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-Do, Republic of Korea
3 Department of Biochemistry, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-Do, Republic of Korea

Correspondence Address:
Ai N. H. Phan
Department of Biochemistry, Wonju College of Medicine, Yonsei University, 20 Ilsan, Wonju, Gangwon-Do 220-701
Republic of Korea
Jong-Whan Choi
Department of Biochemistry, Wonju College of Medicine, Yonsei University, 20 Ilsan, Wonju, Gangwon-Do 220-701
Republic of Korea

Abstract

Background: Polyphenolic phytochemicals are natural compounds, easily found in fruits and vegetables. Importantly, polyphenols have been intensively studied as excellent antioxidant activity which contributes to anticancer function of the natural compounds. Lung cancer has been reported to mainly account for cancer-related deaths in the world. Moreover, epidermal growth factor receptor tyrosine kinase inhibitor (TKI) resistance is one of the biggest issues in cancer treatment, especially in nonsmall cell lung cancer (NSCLC). Even though several studies both in preclinical and clinical trials have showed promising therapeutic effects of polyphenolic compounds in anticancer therapy, the function of the natural compounds in TKI-resistant (TKIR) lung cancer remains poorly studied. Objective: The aim of this study is to screen polyphenolic compounds as potential anticancer adjuvants which suppress TKIR lung cancer. Materials and Methods: Colony formation and thiazolyl blue tetrazolium blue assay were performed in the pair-matched TKI-sensitive (TKIS) versus TKIR tumor cell lines to investigate the therapeutic effect of polyphenolic compounds in TKIR NSCLC. Results: Our data show that equol, kaempferol, resveratrol, and ellagic acid exhibit strong anticancer effect in HCC827 panel. Moreover, the inhibitory effect of most of tested polyphenolic compounds was highly selective for TKIR lung cancer cell line H1993 while sparing the TKIS one H2073. Conclusion: This study provides an important screening of potential polyphenolic compounds for drug development to overcome TKI resistance in advanced lung cancer. Abbreviations used: EGFR: Epidermal growth factor receptor, EMT: Epithelial-to-mesenchymal transition, GTP: Green tea polyphenols, IGF1R: Insulin-like growth factor 1 receptor, MET: Met proto-oncogene, MTT: Thiazolyl blue tetrazolium blue, NSCLC: Non-small cell lung cancer, ROS: Reactive oxygen species, RTK: Receptor tyrosine kinase, STAT3: Signal transducer and activator of transcription 3, TKIR: TKI-resistant, TKIs: Tyrosine kinase inhibitors, TKIS: TKI-sensitive.



How to cite this article:
Jeong H, Phan AN, Choi JW. Anti-cancer effects of polyphenolic compounds in epidermal growth factor receptor tyrosine kinase inhibitor-resistant non-small cell lung cancer.Phcog Mag 2017;13:595-599


How to cite this URL:
Jeong H, Phan AN, Choi JW. Anti-cancer effects of polyphenolic compounds in epidermal growth factor receptor tyrosine kinase inhibitor-resistant non-small cell lung cancer. Phcog Mag [serial online] 2017 [cited 2022 Oct 2 ];13:595-599
Available from: http://www.phcog.com/text.asp?2017/13/52/595/218126


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Summary

The study provides an important screening of potential polyphenolic compounds for drug development to overcome tyrosine kinase inhibitor (TKI) resistance in advance lung cancerEquol, kaempferol, resveratrol, and ellagic acid show strong anticancer effect in HCC827 panel, including TKI-sensitive (TKIS) and TKI-resistant clonesThe inhibitory effect of polyphenolic compounds such as equol, kaempferol, resveratrol, ellagic acid, gallic acid, p-Coumaric, and hesperidin is highly selective for TKI-resistant lung cancer cell line H1993 while sparing the TKIS one H2073.

 Introduction



Lung cancer is the highest cause of cancer deaths in the world.[1] The initiation of lung cancer is induced by diverse oncogenic activation and tumor suppressor inhibition. Receptor tyrosine kinase epidermal growth factor receptor (EGFR) is usually strongly active in non-small cell lung cancer (NSCLC) and regulates various important tumorigenic processes.[2] Targeting EGFR signaling, using tyrosine kinase inhibitors (TKIs) such as gefitinib or erlotinib, provides dramatic survival benefit for EGFR-mutant lung cancer patients.[3] However, majority of patients, initially responsive to TKI treatment, eventually develop TKI resistance and tumor relapse.[4] Molecular mechanisms of acquired TKI resistance in EGFR-mutant NSCLC are vary from patients to patients, due to the biological heterogeneity among tumor cells existing before treatment and continually increasing through selection pressure of the treatment. EGFR secondary mutation T790M is among the most popular TKI-acquired resistant mechanisms. The mutation prevents TKIs, such as gefitinib and erlotinib, to bind the kinase cleft of EGFR and reduces drug effectiveness.[4] Other tracks bypassing EGFR signaling account for 20% of TKI-resistant (TKIR) mechanism, such as amplification of the met proto-oncogene (MET), activation of insulin-like growth factor 1 receptor, feedback activation of signal transducer and activator of transcription 3 (Stat3), Kras mutations, or epithelial-to-mesenchymal transition.[5] Different therapeutic approaches to overcome TKI resistance in lung cancer have been established, such as development of next generations of TKIs (CO-1686 and AZD-9291), combination of surgery and radiation therapy for the region surgically removed, or combination of radiation therapy and chemotherapy.[4] However, despite advances in early prognosis and standard therapy, prevention and treatment strategies for advanced lung cancer are unmet needs, especially to overcome TKI resistance.

It has been reported that dietary optimization is among the most effective approaches for cancer prevention.[6] Importantly, about 20% of all cases of cancer are preventable by modified diet containing high amount and variety of vegetables and fruits.[7] Polyphenolic phytochemicals are natural compounds highly contained in fruits, vegetables, and cereal and involved in protecting plants from microbial infections, deterrence of herbivores, preventing reactive oxygen species (ROS) stress, regulation of growth processes, and ripening.[6] Polyphenol structure is characterized by the presence of multiphenol units, which might contribute to oxidative stability of plant tissue and other organoleptic characteristics, such as color, flavor, and odor.[6] Due to favorable safety profile and profound antioxidant activity, polyphenolic phytochemicals have been intensively studied as anticancer adjuvants.[8],[9],[10] Particularly, in mice-harboring mammary carcinoma 4T1, green tea polyphenols dramatically suppressed cancer development and inhibited tumor metastasis.[11] Furthermore, a clinical study on patients with intestinal premalignant lesions showed that 6-month treatment of quercetin and curcumin inhibited the development of polyps both in number and size.[12] Moreover, in various epidemiological studies, consumption of fruits and vegetables with high content of lycopene reduces risks of cancer development in prostate, alimentary tract, and cervix.[13],[14],[15] Even though polyphenolic phytochemicals showed promising effect in anticancer therapy both in preclinical and clinical studies, therapeutic effect of the natural compounds in EGFR-TKI-resistant lung cancer remains poorly studied. Here, our study investigated the anticancer effect of a set of polyphenolic phytochemicals on TKIR lung cancer cell lines. Interestingly, we found that most tested phytochemicals showed profound effect to suppress TKIR NSCLC. This study, therefore, provides a fundamental screening of potential natural compounds as adjuvants which might be included in the treatment combo to overcome TKIR NSCLC.

 Materials and Methods



Cell lines and reagents

HCC827, HCC827C1, HCC827C2, H2073, and H1993 cells were a kind gift of Dr. John D. Minna (University of Texas Southwestern Medical Center, Dallas, Texas, US). All cells were grown in 5% fetal bovine serum-supplemented RPMI 1640, at 37°C and 5% CO2 atmosphere.

Polyphenolic compounds, including (+)-catechin hydrate, caffeic acid, chlorongeic acid, ellagic acid, equol, gallic acid, hesperidin, kaempferol, p-Coumaric acid, quercetin dihydrate, resveratrol, and shikimic acid were from Sigma.

Colony formation assay

About 3000 cells/well were seeded into 6-well plates containing RPMI medium in final volume of 2 mL/well. After 24 h, cells were incubated with indicated polyphenolic compounds for 7 days. To visualize the colonies, cells were stained with methylene blue solution (0.4% in methanol 50%).

Thiazolyl blue tetrazolium blue assay

About 1000 cells/well were splitted into 96-well microplates containing RPMI medium in final volume of 0.1 mL/well. After 24 h, cells were incubated with indicated polyphenolic compounds. Five days after treatment, thiazolyl blue tetrazolium blue (MTT) from Sigma was used to measure cell viability.

Statistical analysis

The data are showed as mean ± standard error of the mean two-way ANOVA was used to assess the significant difference in MTT assays in [Figure 1]. The difference between viability of H1993 and H2073 treated with a single dose in [Figure 1] was examined by two-tailed unpaired t-test. *, P < 0.05;Δ, P < 0.01;#, P < 0.001.{Figure 1}

 Results



Therapeutic effect of polyphenolic phytochemicals on HCC827 panel

The chemical structures and molecular weight of tested polyphenolic phytochemicals are represented [Figure 2] and [Table 1]. Structurally, the polyphenolic compounds are classified into three groups of phenolic acids, flavonoids, and stilbenes. Shikimic acid, p-coumaric acid, ellagic acid, gallic acid, caffeic acid, and chlorogenic acid are included in phenolic acid class; flavonoids consist of (+)-catechin hydrate, equol, kaempferol, queretin dihydrate, and hesperidin; and resveratrol is a stilbene compound. Most of the polyphenolic compounds arise from a common precursor, shikimic acid.[6] Principally, they appear in conjugated structures, with one or more sugar molecules linked to hydroxyl groups. The hydroxyl groups in polyphenolic compounds can uptake free electrons to form a stable phenoxyl radicals that subsequently interrupts cellular oxidative reaction and reduces ROS in the cells.[6]{Figure 2}{Table 1}

To explore therapeutic function of polyphenolic phytochemicals on TKIR lung cancer, we first used a panel of NSCLC cells including parental TKI-sensitive (TKIS) cells HCC827 and TKIR clones HCC827C1 and HCC827C2. As previous described, parental HCC827 cells, harboring active mutation EGFRE746-A750del, are very sensitive to TKIs, while HCC827C1 and HCC827C2 are resistant to TKI treatment.[16] To investigate inhibitory effect of polyphenolic compounds on HCC827 panel, we carried out colony formation assay in a dose-dependent manner [Figure 3]. Interestingly, we found that equol, kaempferol, resveratrol, and ellagic acid dramatically suppressed cell growth of HCC827C2 [Figure 3]a. On the other hand, chlorogenic acid, hesperidin, caffeic acid, and queretin dihydrate showed strong inhibitory effect on HCC827C2 growth only at 200 μM [Figure 3]a. (+)-Catechin hydrate, shikimic acid, and p-Coumaric acid did not show any growth inhibitory effect on HCC827C2 [Figure 3]a. We next tested growth response of parental HCC827 and HCC827C1 to equol, kaempferol, resveratrol, and ellagic acid treatment. Similar to HCC827C2, liquid colony forming assay showed that the compounds strongly suppressed cell growth of HCC827 and HCC827C1 [Figure 3]b and [Figure 3]c. These data provide a systemic screening of polyphenolic compounds that strongly sensitize TKIR lung cancer cells.{Figure 3}

Therapeutic effect of polyphenolic phytochemicals on H2073 and H1993

We next tested therapeutic effect of some screened polyphenols in a panel of cancer cells including H2073 and H1993. Note that H2073 and H1993, respectively, are primary and metastatic tumor cells established from the same patient as previous described.[17] Mechanically, H2073, with overexpression of EGFR, is highly sensitive to TKI treatment, whereas H1993-harboring MET amplification is strongly resistant to TKIs.[17] We then tested growth inhibition of H2073 and H1993 cells by the polyphenolic phytochemicals which can suppress growth of HCC827 parental and the TKIR clones as described above. Surprisingly, we found that most phytochemicals sensitized the TKIR lung cancer cells H1993 which showed minor suppressive effect on H2073 growth. Particularly, equol, kaemferol, resveratrol, and ellagic acid strongly inhibited H1993 in a dose-dependent manner, while H2073 did not significantly respond to the compounds' treatment [Figure 1]a,[Figure 1]b,[Figure 1]c,[Figure 1]d. A recent study has reported that gallic acid showed strong inhibitory effect, both in vitro and in vivo, on cell growth of TKIR lung cancer, while sparing other TKIS cells.[16] We then tested the viability response of H2073 and H1993 to gallic acid treatment. Consistently, we found that H1993 is extremely sensitive to gallic acid at 5 μM, while H2073 was not responsive to gallic acid treatment [Figure 1]e. Similarly, hesperidin and p-Coumaric acid strongly inhibited H1993 and showed only modest effect on H2073 [Figure 1]f and [Figure 1]g. Interestingly, even though p-Coumaric acid and hesperidin showed modest effect on HCC827C2 [Figure 3]a, the compounds strongly suppressed cell viability of H1993 at the same treatment condition. In conclusion, our data suggest promising anticancer effects of screened polyphenolic compounds, especially to overcome TKI resistance in NSCLC.

 Discussion



Even though advances in standard treatment and diagnosis techniques have improved patient overall survival recently, emergence of TKI resistance become a serious problem in NSCLC treatment. Moreover, developing new drugs or new targets for cancer treatment remains to be a remarkable clinical challenge both effectively and economically, especially in TKIR NSCLC. Polyphenolic phytochemicals are natural-derived compounds which play critical functions in protecting plants from microbial infections, preventing ROS stress, or deterrence of herbivores.[18],[19],[20] Notably, growing evidence shows that dietary polyphenols such as curcumin, resveratrol, and EGCG exert their chemopreventive effects against different types of cancers in preclinical studies.[21],[22],[23],[24] Intensive studies on antioxidant as well as anticancer activity of polyphenolic phytochemicals suggested supplement of polyphenols in daily diet as a prevention strategy for cancer development.[7],[22] However, therapeutic function of polyphenolic compounds in TKIR NSCLC remains poorly studied.

In the present study, for systemic screening of polyphenolic phytochemicals as anticancer adjuvants in TKIR lung cancer, we firstly selected various polyphenolic compounds from three major classes of polyphenols, including phenolic acid, flavonoid, and stilbene. These compounds were then investigated for therapeutic effect in TKIR lung cancer cells.

Next, we used a panel of HCC827 cell lines including parental cells and two independent TKIR clones HCC827C1 and HCC827C2 to address cancer-suppressing effects of the polyphenolic compounds. Interestingly, we found that equol, kaempferol, resveratrol, and ellagic acid are potent anticancer agents in both HCC827 and TKIR cells. The data, therefore, provide a fundamental screening of polyphenolic compounds to sensitize TKIR NSCLC. We next confirmed growth-inhibitory function of tested natural compounds in another set of lung cancer cells including H2073 and H1993 which are primary and pair-matched metastasis tumor cells, respectively, isolated from the same patient. Note that H2073, harboring overexpressed EGFR, are sensitive to TKI treatment, while H1993, containing amplification of MET, are highly resistant to TKIs.[17] To our surprise, most of test polyphenolic compounds, including equol, kaempferol, resveratrol, ellagic acid, p-Coumaric acid, hesperidin, and gallic acid dramatically suppressed cancer growth of TKIR cells H1993 while sparing TKIS cells H2073. Importantly, gallic acid has been reported in a previous study to specifically inhibit tumor development of TKIR cells but not of TKIS cells, both in vitro and in xenograft model.[16] Consistently, our data showed the selective cancer-suppressive effect of gallic acid in TKIR cells H1993 but not in TKIS H2073 cells. Gallic acid has been suggested to target Src-mediated Stat3 signaling, subsequently suppress TKIR cells specifically.[16] However, the molecular targets of other polyphenolic compounds such as equol, kaempferol, resveratrol, ellagic acid, p-coumaric acid, and hesperidin remain elusive, especially in TKIR cells. Therefore, efforts are required to identify molecular mechanism by which these phytochemicals specifically suppress TKI-resistant NSCLC.

Taken together, our study provides a fundamental yet important screening of potential natural compounds for anticancer drug development, especially to overcome TKI resistance in advanced lung cancer. Therefore, the administration of polyphenolic compounds might serve as a potent adjuvant therapeutic strategy, supporting long-term TKI treatment in lung cancer patients.

Acknowledgement

This study was financially supported by a research grant from Yonsei University Wonju College of Medicine (YUWCM-2008-19), Yonsei University Future-leading Research Initiative of 2015 (RMS2-2015-22-0094), JJ-2017-1, and the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology.

Financial support and sponsorship

This study was financially supported by a research grant from Yonsei University Wonju College of Medicine (YUWCM-2008-19), Yonsei University Future-leading Research Initiative of 2015 (RMS2-2015-22-0094), JJ-2017-1, and the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF-2017R1D1A3B03033851) and (NRF-2016R1D1A3B03930581).

Conflicts of interest

There are no conflicts of interest.

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