EFFECT OF QUERCETIN ON HYPOXIA-REGULATED METASTATIC MARKERS IN AGGRESSIVE PANCREATIC CANCER CELLS UNDER HYPOXIC CONDITIONS

EFFECT OF QUERCETIN ON HYPOXIA-REGULATED METASTATIC MARKERS IN AGGRESSIVE PANCREATIC CANCER CELLS UNDER HYPOXIC CONDITIONS

Phani Bhushan Meka, Hiba Ahmed, Hajera Unissa, Huda Tahera, Mohammad Ahmed Waheed, Maryam Sadiq, Sumayya Afreen and Nazima Begum *

Vimta Labs Ltd, Hyderabad, Telangana, India.

ABSTRACT: Tumor hypoxia is an important pathological condition that influences several signaling cascades in malignant cells, eventually leading to therapy resistance. Several natural bioflavonoids hold promise as anti-cancer agents. However, the effect of Quercetin on hypoxic pancreatic cancer cells is unknown. We analyze the effect of Quercetin on expression levels of metastatic markers HIF1α and E-cadherin under hypoxic conditions. Quercetin treatment was significantly correlated with reduced HIF1α expression levels and elevated E-cadherin levels. Our results suggest that Quercetin may alter E-cadherin levels by regulating HIF1α expression. Quercetin may inhibit pancreatic cancer cell metastasis by regulating metastasis genes in a hypoxic microenvironment and has pharmacological potential in aggressive pancreatic cancer treatment.

Keywords: Quercetin, HIF1α, E- cadeherins, PC 1, N cadherin, Vimentin, Cytokeratins

INTRODUCTION: Pancreatic cancer is an intractable and rare malignancy ranked 12th in incidence and 7th in mortality. It is the leading cause of cancer deaths in developed countries and is rising in developing countries like India. According to  GLOBOCAN 2020 statistics, pancreatic cancer has ranked the 11th most common malignancy in the world and accounts for 495773 new cases and caused 466003 deaths in 2020 ¹. The incidence and mortality of pancreatic cancer have been associated with age and is slightly more common in men than in females. Several risk factors have been found to be associated with the development of pancreatic cancer.

Among lifestyle habits, consumption of alcohol and tobacco abuse are the common causes of malignancy development ²^, ³. Despite advanced therapeutic strategies for pancreatic cancer treatment, the outcome of the therapies is moderate, which might be due to the complex histology and tumor microenvironment of the pancreas. It processes extracellular matrix proteins and non-neoplastic cells like fibroblastic, vascular, and immune cells. Recent studies have reported that the pancreas's stroma supports tumor cell growth, promotes cancer cell dissemination, and simultaneously acts as a physical barrier to drug delivery.

Moreover, a tumor hypoxic microenvironment that arises due to low oxygen supply to a growing tumor may alter patho physiological functions of several genes. Hypoxic tumor microenvironment may contribute to tumor progression, metastasis, and resistance to chemo/radiotherapy ⁴.

Several natural plant products have shown anti-cancer properties influencing tumor cell proliferation and metastasis. Among several naturally occurring compounds, flavonoids are considered promising therapeutic agents against human malignancies. Quercetin (3,3′,4′,5,7- pentahydroxyflavone) is one of the important flavonoids shown to exhibit anti-cancer properties by influencing several intracellular pathways ⁵. Quercetin has been reported to inhibit several cell signaling components in cancer cells, including PI3K/Akt/mTOR, GSK-3β, NFκB, and heat shock protein 70 (HSP70). However, the effect of Quercetin on the regulation of metastatic markers in a hypoxic microenvironment is obscure ⁵.

In our study, we aimed to analyze the effect of Quercetin on the expression of key metastatic regulators such as HIF-1α (Hypoxia-inducible factor 1 alpha), a master regulator of hypoxic microenvironment and E- Cadherin under the chemical induction of hypoxia and Quercetin treatment.

MATERIALS AND METHODS: To study the effect of chemical induction of hypoxia and Quercetin treatment on expression levels of metastatic markers (HIF1α and E cadherin ), we have selected one aggressive pancreatic cell line AsPC1. Cell lines were purchased from NCCS, Pune, and cultured using MEBM/DMEM+10%FBS medium. Subcultures and passages were performed as per standardprotocols ⁶.

Optimization of CoCl2 and Quercetin Treatments on Cell Lines: Various concentrations of CoCl₂ (100 µM, 200µM, and 300µM) were prepared. 2000 cells were seeded in each well along with 100 µl of culture media in a 96-well plate. The experiment was performed in triplicates with three different concentrations of CoCl₂ at three different time periods 24 h, 48 h and 72 h to determine the IC50 value of CoCl₂ on cell line. Cells without CoCl₂ were used as negative control.Cells from different exposures of CoCl₂ were subjected to MTT assay to calculate the proliferation rate. 200µM CoCl₂ concentration significantly reduced cell proliferation rate compared with control cells. Three different concentrations of Quercetin (3 µM, 12 µM, 48 µM) were prepared. Each concentration was applied on cell lines at different time intervals (0, 24, 48, 72 hours). RNA was isolated from treated cell lines using the Trizol method and subjected to cDNA conversion. HIF1α and E- Cadherin Expression analyses were assessed using Real-Time PCR (ABI7500) with Sybr green. Each experiment was carried out in triplicate, and beta-actin as an endogenous control.

RESULTS:

HIF1α and E Cadherin Expression in Control and Hypoxia-Induced as PC1 Cell Line: CoCl₂ treated cell line differed significantly concerning HIF1α levels (1.08±0.01) compared to control (Un treated cell line (0.98±0.004) even before chemical induction of hypoxia. When both cell lines were exposed to hypoxic conditions, HIF1α levels were significantly elevated as the duration of hypoxic exposure increased Table 1.

TABLE 1: HIF1Α EXPRESSION IN CONTROL AND HYPOXIA-INDUCED AS PC1 CELL LINE

TABLE 2: E CADHERIN EXPRESSION IN CONTROL AND HYPOXIA INDUCED AS PC1 CELL LINE

However, the elevation was more prominent after 48 hrs of induction. Before hypoxic induction, E cadherin levels were significantly elevated in the control cell line (1.55±0.01) compared to the treated cell line (1.41±0.01). As the duration of hypoxic exposure increased, the E cadherin levels gradually decreased in both treated and control cell lines. The comparison between treated and control cell lines indicated that response was maximum after 24 hrs in the normal cell line but only after 72 hrs in the tumor cell line Table 2.

HIF1α and E Cadherin Expressions in Quercetin are Treated as PC1 Cell Line: HIF1α levels were significantly decreased in both cell lines during 48 hours and 72 hours of quercetin exposure at 3µM concentrations. On 24 hours of treatment, both cell lines did not show a significant decrease concerning HIF1α levels Fig. 1.

However, HIF1α levels steeply declined in the normal cell line compared to tumour cell line at 3µM quercetin concentrations during 48 hours and 72 hours of exposure. E cadherin levels were gradually increased as the duration of quercetin exposure increased in cancer cell lines. E cadherin levels were significantly different between the two cell lines. However, in normal cell lines, E cadherin levels were significantly increased at 3 µM concentration for 24, 48, and 72 hours. Other concentrations did not show exerted influence concerning E cadherin levels in 24, 48, and 72 hours Fig. 2.

FIG. 1: 3 HIF1Α EXPRESSION IN QUERCETIN TREATED AS PC1 CELL LINE          

FIG. 2: E CADHERIN EXPRESSION IN QUERCETIN TREATED AS PC1 CELL LINE

DISCUSSION: Hypoxia or low oxygen concentration is a salient feature of solid tumours. Under hypoxic microenvironment, tumour cells are deficient in oxygen and nutrients due to impaired vasculature which fails to supply adequate oxygen/nutrients to the growing tumour cells. The hypotic microenvironment regulates several cell signaling pathways by regulating crucial genes that play an important role in angiogenesis, metastasis and proliferation.

HIF-1α (Hypoxia-inducible factor 1 alpha), is a transcription factor that regulates nearly 150 genes that influence tumor cell development and progression. HIF-1 α levels are increased in a hypoxic microenvironment which further promotes angiogenesis. Therefore, tumor cells get oxygen and nutrients for growing cells. Increased expression of HIF-1 α has been associated with elevated microvessel density and aggressive tumor phenotype ⁷. HIF-1 α gene mediates the E cadherin gene function and influences cancer cell invasion/ mobility ⁶.  Hypoxic tumor cells exhibit resistance to chemotherapeutic agents, resulting in a poor outcome for patient ⁴. Several natural plant components may potentially affect cancer cells and have a favorable outcome. Quercetin is a versatile molecule with many pharmacological properties including antioxidant, neurological, antiviral, anti-cancer, cardiovascular, antimicrobial, anti-inflammatory, hepatoprotective and anti-obesity agents.

Earlier studies reported that quercetin may influence HIF1a activity ⁸. In our study, we observed that HIF-1 α expression levels were significantly decreased under Quercetin treatment in chemically induced hypoxic pancreatic cell lines. The levels of HIF-1 α were decreased as the concentration and duration of Quercetin increased.  Our results were by previous reports where HIF-1 α levels are decreased upon Quercetin treatment in LNCaP prostate cancer cells, CX-1 colon cancer cells, and SkBr3 breast cancer cells ⁸. Further, the E-cadherin gene expression levels were significantly elevated in Quercetin-treated pancreatic cells. Previously, it was shown that Quercetin can inhibit EMT by increasing E-cadherin expression and decreasing the N-cadherin, Vimentin, Snail protein family in many cancers ⁹.

Decreased HIF-1 α levels might result in the accumulation of E-cadherin in chemically induced hypoxic cells. Zhu et al, reported that HIF 1α inhibition by HIF 1α Homo 1216 siRNA transfection repressed hypoxia-induced HIF 1α, RGC 32, N cadherin, and vimentin, but elevated the levels of E cadherin and cytokeratins.

In conclusion, Quercetin treatment is significantly associated with decreased levels of HIF-1 α and elevated E-cadherin expression in aggressive pancreatic cell lines, suggesting that Quercetin might have potential pharmacological application for the treatment of aggressive pancreatic cancer.

ACKNOWLEDGEMENTS: This work was supported by Vimta Labs

CONFLICTS OF INTEREST: All the authors declare that they have no conflicts of interest.

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   How to cite this article:

   Meka PB, Ahmed H, Unissa H, Tahera H, Waheed MA, Sadiq M, Afreen S and Begum N: Effect of quercetin on hypoxia regulated metastatic markers in aggressive pancreatic cancer cells under hypoxic conditions. Int J Pharm Sci & Res 2023; 14(3): 1507-10. doi: 10.13040/IJPSR.0975-8232.14(3).1507-10.

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