Skip to main content

A novel nitidine chloride nanoparticle overcomes the stemness of CD133+EPCAM+ Huh7 hepatocellular carcinoma cells for liver cancer therapy



Stemness of CD133+EPCAM+ hepatocellular carcinoma cells ensures cancer resistance to apoptosis,which is a challenge to current liver cancer treatments. In this study, we evaluated the tumorcidal activity of a novel nanoparticle of nitidine chloride (TPGS-FA/NC, TPGS-FA: folic acid modified D-α-tocopheryl polyethylene glycol 1000 succinate, NC: nitidine chloride), against human hepatocellular carcinoma (HCC) cell line Huh7 growth in vitro and in vivo.


Huh7 cells were treated with TPGS-FA/NC. Cell proliferation was assessed using MTT and colony assays. The expression of cell markers and signaling proteins was detected using western blot analyses. A sphere culture technique was used to enrich cancer stem cells (CSC) in Huh7 cells. TPGS-FA/NC (7.5, 15, 30, 60, 120 μg/mL) dose-dependently inhibited the proliferation of HCC cells, which associated with a reduction in AQP3 and STAT3 expression. Importantly,TPGS-FA/NC (10, 20, and 40 μg/mL) significantly reduced the EpCAM+/CD133+cell numbers, suppressed the sphere formation. The in vivo antitumor efficacy of TPGS-FA/NC was proved in Huh7 cell xenograft model in BALB/c nude mice, which were administered TPGS-FA/NC(4 mg· kg − 1· d − 1, ig) for 2 weeks.


TPGS-FA/NC dose-dependently suppressed the AQP3/STAT3/CD133 axis in Huh7 cells. In Huh7 xenograft bearing nude mice, TPGS-FA/NC administration markedly inhibited Huh7 xenograft tumor growth .


TPGS-FA/NC inhibit HCC tumor growth through multiple mechanisms, and it may be a promising candidate drug for the clinical therapy of hepatocellular carcinoma.

Peer Review reports


Multiple drugs have been used broadly in liver cancer therapy, but their water-insolubility and toxicity have raised serious concerns [1, 2]. Nitidine chloride has been developed in the past two decades due to its promise pharmacological action. However, Nitidine chloride have limited applications because of potential organ damage, hypersensitivity, and neurotoxicity [3, 4]. Thus, facing the liver cancer therapy challenge, it is urgent to discover promising drug target and methods to achieve safe and effective tumor inhibition.

The cancer stem cells(CSC) are identified as stem cell properties,which revealed the existence of CSC in HCC [5, 6]. Intriguingly, CD133+EpCAM+phenotype precisely represented the characteristics of CSC in Huh7 cells [7,8,9,10,11]. Currently some chemotherapeutic drugs primarily inhibit the growth of differentiated tumor cells with no impact on CSC [12, 13]. Cancer stem cells (CSCs) maintain the stemness to ensure their survival and growth, and becoming resistant to current treatments [14,15,16]. The intrinsic pathway of CD133+Huh7 cells is regulated by the AQP3 protein in the progression and metastasis of several malignant tumors [17,18,19,20]. Furthermore, Nek2 is the critical regulator of the centrosome, making hepatocellular carcinoma more resistance to current treatments [21, 22]. In this regard, functional AQP3 and Nek2 is mutated or highly expressed in hepatocellular carcinoma, these molecular and cellular mechanisms may be overcome by the pharmacological action of AQP3/STAT3/CD133 pathway degradation and Nek2 inhibition. Thus, in this study, we comprehensively investigated the role of TPGS-FA/NC in the antitumor effect and explore its mechanisms via AQP3/STAT3/CD133 axis, which would offer therapeutic strategies against liver cancer.



TPGS-FA/NC was synthesized in our laboratory and dissolved in DMSO. DMEM was purchased from Life Technologies (AB & Invitrogen)(Gibco, Suzhou, China). Fetal bovine serum (FBS) was purchased from Gemini (Gemini Calabasas, CA, USA). Huh7 cells were purchased from Procell Life Science & Technology Co. Ltd. on July 11, 2019 (Wuhani, China). L-02 cells were purchased from Procell Life Science & Technology Co. Ltd. on January 18, 2019 (Wuhani, China). Recombinant human bFGF (bFGF), recombinant human 1epidermal growth factor (EGF) and MTT were purchased from Beijing Solarbio Science & Technology Co., Ltd.(Solarbio,Beijing, China). B27 (× 50) were purchased from Thermofish Scientific(Thermofish,waltham, USA). DMEM/F-12, insulin-Transferrin-Selenium (ITS× 100), L-glutamine (× 100) were purchased from Procell Science&Technology Co.,Ltd.(Procell,Wuhan, China). Anti-CD133 (AC133)-phycoerythrin (PE) and anti-CD326 (EpCAM)-allophycocyanin (APC) antibodies and isotype-matched mouse anti-IgG1-PE and anti-IgG1-APC were purchased from MiltenyiBiotec (North Rhine-Westphalia, Germany). Anti-phosphoSTAT3 (Tyr705), STAT3, JAK1, JAK2, AQP3, EpCAM, NEK2 were purchased from the Beijing Solarbio Science & Technology Co., Ltd. (Solarbio,Beijing, China). Anti-CD133 and anti-GAPDH were purchased from the Proteintech Science&Technology Co.,Ltd.(Proteintech, suzhou, China). Anti-rabbit secondary antibodies were purchased from Thermo Fisher Scientific Science&Technology Co.,Ltd.(Thermo Fisher Scientific, Shanghai, China). DAPI was obtained from Shanghai Beyotime Biotechnology Co. Ltd. (Beyotime,Shanghai, China). The iFluor TM 647 phalloidin iFluor™ were purchased from Yeasen Biotechnology Co., Ltd. (Yeasen,Shanghai, China). 5-fluorouracil (5-Fu) was purchased from MedChemExpress (MCE, Monmouth Junction, NJ, USA).

Cell culture

Huh7 cells and normal hepatic cell line L-02 were cultured in DMEM 10% FBS containing 10% FBS, 100 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C in a humidified 5% CO2 incubator.

Tumor sphere formation assay and flow cytometric analysis

Primary sphere cells were obtained by culturing Huh7 cells in sphere-forming conditioned DMEM/F12, supplemented with FGF (20 ng/mL), EGF (20 ng/mL), B27 (1×), and L-glutamine (1×) in 6-well ultra-low attachment plates The primary sphere cells (1 × 103 cells/well) were incubated with or without TPGS-FA/NC for 7d. The second and third passages of the cells were grown for 7 d in the absence of TPGS-FA/NC. To examine TPGS-FA/NC effects on the subpopulation of cells that expressed EpCAM and CD133, cells were incubated with anti-AC133-PE and anti-EpCAM-APC antibodies and analyzed by flow cytometry. Isotype-matched mouse anti-IgG1-PE and anti-IgG1-APC were used as controls.

Confocal microscopy imaging

Huh7 cells cells were seeded on glass cover-slips and cultured at 37 °C overnight. Rhodamine B isothiocyanate 540 labeled TPGS-FA/NC were incubated with cells at a final concentration of 100 nM for 4 h at 37 °C. After washing twice with PBS buffer, cells were fixed with 4% formaldehyde and washed again, followed by treatment with 0.1% Triton X-100 in PBS buffer for 5 min and subsequent cytoskeleton staining with iFluor TM 647 phalloidin iFluor™ for 30 min at room temperature. Containing DAPI for cell nucleus staining and assayed on Leica SP8 confocal microscope (Leica Corp.).

Western blotting

Cells were lysed in RIPA lysis buffer with PMSF and protease in-hibitors. Total protein lysates were boiled with loading sample buffer containing 8% SDS-PAGE. Separated proteins were transferred onto PVDF membranes. PVDF membrane blots were blocked in 10% skimmed milk for 0.5-1 h at room temperature, washed in Tris-buffered saline with Tween 20 (TBS-T) and incubated overnight at 4 °C with rabbit anti-phosphoSTAT3 (Tyr705), anti-STAT3, anti-JAK1, anti-JAK2, anti-AQP3 CD33, anti-GAPDH. Anti-rabbit IgG was used as the second antibody.

Immunohistochemistry (IHC)

AQP3/CD133/EPCAM/NEK2 expression was analyzed in paraffin-embedded specimens obtained from nude mice tumor tissue. Tissue sections were incubated with anti-AQP3 (1:100, Solarbio), anti-CD133 (1:100, Solarbio), anti-EPCAM (1:100, Solarbio), and anti-NEK2 (1:100, Solarbio) overnight at 4 °C. Then, the sections were incubated with biotinylated goat anti-rabbit IgG as a secondary antibody (Zhongshan Kit, China) for 30 min at 37 °C. The specimens were assessed three times.

In vivo biodistribution assay

Rhodamine B isothiocyanate labeled TPGS-FA/NC (2− 1, NC per body weight) were systemically administered via the tail vein into Huh7 tumor bearing mice. PBS-injected mice were used as fluorescence negative controls. The whole-body imaging of mice was conducted at 8 h using an IVIS system (XMRS) with excitation at 535 nm and emission at 694 nm. The mice were sacrificed at 8 h post-injection by the inhalation of CO2 followed by cervical dislocation, and major organs were collected and subjected to fluorescence imaging for the assessment of biodistribution profiles. The fluorescence imaging datas of average radiant efficiency ([ps− 1cm− 2sr− 1] [μWcm− 2] − 1) were quantitative by IVIS system (XMRS) program.

Magnetic-activated cell sorting assay

Determine cell number,Centrifuge cell suspension at 300×g for 10 minutes, Aspirate supernatant completely. Resuspend cell pellet in 300 μL of buffer per 5 × 107 total cells. Add 100 μL of FcR Blocking Reagent per 5 × 107 total cells and mix well. Add 100 μL of EpCAM microbeads per 5 × 107 total cells. Mix well and incubate for 30 minutes (2 − 8 °C). Wash cells by adding 5 − 10 mL of buffer per 5 × 107 cells and centrifuge at 300×g for 10 minutes. Aspirate supernatant completely and suspend up to 106 cells in 500 μL buffer, proceed to magnetic separation, EpCAM Huh7 cells were collected. Followed above methods, EpCAM Huh7 cells were sorted after CD133 microbeads incubation. EpCAM+and CD133+Huh7 cells were collected by magnetic separation.

In vivo tumor inhibition by TPGS-FA/NC nanoparticles

Freshly sorted EpCAM+ CD133+ Huh7 cells were collected in sterile DMEM without FBS. 1 × 107 Huh7 cells/site cell suspension, mixed with matrigel (BD Biosciences, CA) (1:1), was subcutaneously injected into the axillary of nude mice, which were randomly divided into four groups (n = 5 biologically independent animals). When the tumor nodules had reached a volume of 75 mm3, the nude mouse were used for tumor inhibition studies. Samples were administrated by i.v. injection in a total of 5 doses (4 mg kg− 1, NC per body weight) every other day. Tumor volume, calculated as (length×width2)/2, and mouse weight were monitored every other day. Data were statistically analyzed by two-tailed unpaired t-test and presented as mean ± SD; *p < 0.05; **p < 0.01; ***p < 0.001.


Statistical differences were evaluated using two-tailed unpaired t-test with GraphPad software, and statistically significant differences are denoted as *p < 0.05, **p < 0.01, and ***p < 0.001. No adjustments were made for multiple comparisons.


TPGS-FA/NC inhibited cell proliferation and targeted the Huh7 cells

We found that Huh7 cells (2 × 103cells/well) were seeded into 96-well plates and treated with TPGS-FA/NC (0–120 μg/mL) for 24, 48, and 72 h (Fig. 1). Cell proliferation was assessed using MTT in a concentration- and time-dependent manner. To evaluate nanoparticles targeting tumor capability, the RhodamineB isothiocyanate 540 fluorophore was attached to TPGS-FA. Confocal microscope imaging showed that TPGS-FA/NC nanoparticles entered the Huh7 cells in vitro, compared with the control groups (Fig. 2).

Fig. 1
figure 1

The effect of TPGS-FA/NC on Huh7 cell proliferation (a) Chemical structure of NC (b) TPGS-FA/NC nanoparticles. c-e In vitro cytotoxicity study of TPGS-FA/NC by MTT assay in 24, 48 and 72 h. (Data are presented as mean ± SD n = 3 independent samples)

Fig. 2
figure 2

In vitro Huh7 cells binding of TPGS-FA/NC nanoparticles. Fluorescence staining of Huh7 cells, which were treated withTPGS-FA/NC for 48 h, was visualized by fconfocal microscopy. (blue: nucleus; green: cytoskeleton; red: TPGS-FA/NC nanoparticles. Scale bar: 50 μm for original images, and 10 μm for magnified image)

TPGS-FA/NC reduced hepatic cancer stem-like cells

To investigate whether TPGS-FA/NC suppressed hepatic CSCs, we enriched the hepatic CSC populations in the Huh7 cell lines using the sphere culture technique. The flow cytometric analysis demonstrated that the EpCAM+/CD133+ cells accounted for 82.0% of the Huh7 sphere cells, respectively. TPGS-FA/NC (10、20 and 40 μg/mL) potently reduced the fraction of EpCAM+/CD133+ cells (Fig. 3a).

Fig. 3
figure 3

The effect of TPGS-FA/NC on hepatic cancer stem-like cells. a TPGS-FA/NC reduced the population of EpCAM+/CD133+ cells for 48 h. Data are presented as mean ± SD and **p < 0.01 and ***p < 0.001. b TPGS-FA/NC reduced the sizes Huh7 primary spheres (magnification,× 400). c Phase contrast photomicrographs obtained by normal hepatocyte cell L-02 treated with TPGS-FA/NC at a concentration of 40 μg/mLfor 48 h (magnification,× 100)

TPGS-FA/NC inhibited hepatoma cell proliferation and colony formation

To test whether TPGS-FA/NC could sense the clonogenic assays, HCC cells (1 × 103cells/well) were treated with or without TPGS-FA/NC in 6-well ultra-low attachment microplates and allowed to grow for 17 to 21 days. Importantly, the treatment inhibited Huh7 cell proliferation and also markedly reduced the number of colonies (Fig. 3b). Intriguingly, compared with control, TPGS-FA/NC showed no adverse effect in normal hepatic cell line L-02 by 40 μg/mL TPGS-FA/NC treatment (Fig. 3c).

TPGS-FA/NC suppressed the AQP3 /CD133/STAT pathways

Next, we set out to expore the mechanism of TPGS-FA/NC on AQP3 /CD133/STAT axis inhibittion. We found that TPGS-FA/NC reduced the protein expression levels of JAK1, JAK2, pY705-STAT3, STAT3 (Fig. 4). Furthermore, TPGS-FA/NC reduced the AQP3 protein expression, which suppressed the expression of activated STAT3 (pY705-STAT3) (Fig. 4). Then, in vivo experiment, we set out to test the CD133 and AQP3 expression levels in sections of nude mice subcutaneous tumors by IHC. Collectively, these results signified that TPGS-FA/NC downregulated AQP3 and CD133 protein levels (Fig. 5).

Fig. 4
figure 4

TPGS-FA/NC inhibits the AQP3/STAT3/CD133 pathway in Huh7 cells. Huh7 cells were treated with the indicated TPGS-FA/NC concentrations for 48 h. Western blotting was performed to determine the AQP3/STAT3/CD133 signaling-associated protein levels

Fig. 5
figure 5

TPGS-FA/NC suppresses the protein levels in Huh7 xenograft specimens. a, b The protein of AQP3, NEK2,EPCAM, and CD133 (× 400, 40 μm) were mainly located in cytomembrane by immunohistochemical assay in 20 HCC mice bearing Huh7 xenograft specimens(**p < 0.01) n = 3. Mean ± SD. * P < 0.05 vs control. # P < 0.05 vs TPGS-FA/NC

TPGS-FA/NC impaired NEK2/CD133/EpCAM signaling of HCC

Next, the protein levels of NEk2,CD133 and EpCAM were determined in cells and nude nice treated with and without TPGS-FA/NC. TPGS-FA/NC successfully reduced protein expression levels of NEk2, CD133 and EpCAM in HCC. In vivo experiment, we tested the CD133 and AQP3 expression levels in sections of nude mice subcutaneous tumors by IHC. Together, these results suggest that TPGS-FA/NC downregulated NEk2, CD133 and EpCAM protein levels (Fig. 5).

In vivo significant inhibition of tumor by TPGS-FA/NC nanoparticles

Thinking from a therapeutic notion, We then Tumor quantitative biodistribution and targeting of TPGS-FA/NC were assessed, which were injected through the tail vein in vivo. Those images of mice 8 h post-injection showed that the TPGS-FA/NC nanoparticles markedly accumulated in tumor, with low or no accumulation in brain, heart,spleen. (Fig. 6a). Quantitative analysis of the organ images showed strongly tumor accumulation. (Fig. 6b). After injecting with TPGS-FA/NC at a dose of 4 mgkg− 1 (NC per mouse weight) every 2 days for a total of five dosages, the results revealed a inhibitory capability in vivo as administration by tumor volumes, whereas control group (Fig. 6c). The specific tumor inhibition was further confirmed from the tumors harvested after 2-week post injections (Fig. 6d). Of note, the effects of those nanoparticles were biocompatible, suggesting no obvious organ toxicity over two-week post injections (Fig. 7).

Fig. 6
figure 6

a. Representative organ images showing specific tumor targeting of rhodamine B isothiocyanate labeled TPGS-FA/NC nanoparticles 8 h post-injection into mice bearing Huh7 xenograft (T: tumor, Li: liver, H: heart, L: lung, K:kidney, S: spleen, and B:brain; Color scale: radiant efficiency, [p s− 1 cm− 2 sr− 1] [μWcm− 2]− 1). V b. Quantitative analysis of biodistribution in tumors and normal organs, quantified from the organ images. Intravenous treatment of nude mice bearing orthotopic Huh7 xenografts with TPGS-FA/NC nanoparticles (red) and control groups (turquoise: NC, fuchsia:5-Fu, blue: PBS) every other day for a total of five injections (4 mg kg − 1,NC per body weight, indicated by arrows). c. Mice body weight was monitored during the time course of treatments (n = 5 biologically independent animals, statistics was calculated by two-tailed unpaired t-test presented as mean ± SD, *p < 0.05, **p < 0.01, ***p < 0.001, p = 4.3 × 10− 3,3.4 × 10− 3 and 5.0 × 10− 4 comparing TPGS-FA/NC to NC,5-Fu and PBS, respectively). d. Representative images of liver cancer tumors harvested from mice after treatments *p < 0.05, **p < 0.01, ***p < 0.001; p = 0.01, 8 × 10 − 4,and 2 × 10 − 4 comparing TPGS-FA/NC to NC, 5-Fu, and PBS, respectively. Source data are provided as a Source Data file

Fig. 7
figure 7

Representative H&E staining of HCC mice bearing Huh7 xenograft specimens


Recently it has been shown that nitidine chloride (NC) inhibits the growth of many human cancer cells via induction of cell apoptosis [23]. In this study, we modify nitidine chloride to achieve a novel nitidine chloride nanoparticle using TPGS-FA carriers. TPGS(D-α-tocopheryl polyethylene glycol 1000 succinate) is a very safe biocom-patible and safe agent that can efficiently for use as a drug solubilizer [24,25,26]. Consistently, these results suggest no adverse effects of mice injected with TPGS-FA/NC. Importantly, this study provideda new target or method in treatment of hepatocellular carcinoma.

Interestingly, we observed TPGS-FA/NC significantly inhibited Huh7 cellular proliferation and colony formation. Importantly, normal hepatic cell line L-02 were not affected by 40 μg/mL TPGS-FA/NC treatment. Moreover, We examined a targeting effect of TPGS-FA/NC for hepatoma cells. Interestingly, it has been shown the use of the sphere culture technique and flow cytometry to enrich characterize hepatic CSCs [10, 11, 27]. Consistent with previous studies [11], Huh7 sphere cells exhibited CSC membrane biomarkers (EpCAM and CD133) including cell self-renewal capacities. In addition, we have shown that that the TPGS-FA/NC treatment markedly reduced the positive EpCAM/CD133 cell fraction as examined by FACS analysis, which suggested to be related with a suppressed self-renewal capability of these cancer stem-like cells. Meanwhile, we revealed that TPGS-FA/NC markedly reduced the numbers and sizes of the spheres. Moreover, TPGS-FA/NC (4 mg/kg) administration for 14d notably inhibited Huh7 xenograft tumor growth. Based on preliminary work, we reveals that the potential contribution of TPGS-FA/NC may serve as a promising drug in preventing and treating liver cancer.

AQP3/STAT3/CD133 pathway is a novel mechanism in the signal protein expression related to cell proliferation, transcription and survival [16]. AQP3/STAT3/CD133 signaling plays a major role during tumor progression in HCC [16]. Recently, AQP3 has been shown to express in various cancer cells including multiple cancer tissues from stomach, colon, and lung [28,29,30]. Meanwhile, Nek2 is reported to inhibit cancer cell proliferation and promote tumorigenesis and progression in HCC and colon cancer [31]. Consistent with these studies, we showed that TPGS-FA/NC suppressed the AQP3/STAT3/CD133 pathway and Nek2 expression in HCC cells, which was evidenced by reduced overexpression of AQP3 and STAT3, as well as downregulating the expression of CD133 through attenuating the stemness of CD133+ cells. Therefore, the downregulation of the AQP3/STAT3/CD133 pathway may be have contributed to the inhibitory effect of TPGS-FA/NC on HCC cells and hepatic CSCs.


In conclusion, we have shown that TPGS-FA/NC is an effective inhibitor of HCC tumor growth with low toxicity. Furthermore, this study demonstrates that TPGS-FA/NC suppresses hepatoma cell proliferation and hepatic CSCs, as well as the AQP3/STAT3/CD133 axis and Nek2 expression in offering possible multiple mechanisms for its antitumor activity. Further clinical works are warranted to investigate the long-term effects of TPGS-FA/NC on tumor metastasis control and extending the patient’s survival .

Availability of data and materials

All data generated or analyzed during the present study are included in this article. Supplementary data are present in the supplemental materials. Additional data related to this paper can be requested from the author (


  1. Spencer CM, Faulds D. Paclitaxel. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the treatment of cancer. Drugs. 1994;48:794–847.

    Article  CAS  Google Scholar 

  2. Rowinsky EK, Donehower RC. Paclitaxel (taxol). N Engl J Med. 1995;332:1004–14.

    Article  CAS  Google Scholar 

  3. Li L, Tu M, Yang X, Sun S, Wu X, Zhou H, et al. The contribution of human OCT1, OCT3, and CYP3A4 to nitidine chltoxicity. Drug Metab Dispos. 2014;42:1227–34.

    Article  Google Scholar 

  4. Li LP, Song FF, Weng YY, Yang X, Wang K, Lei HM, et al. Role of OCT2 and MATE1 in renal disposition and toxicity of nitidine chloride. Br J Pharmacol. 2016;173:2543–54.

    Article  CAS  Google Scholar 

  5. Jemal A, Bray F, Center MM, et al. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90.

    Article  Google Scholar 

  6. Zhou BB, Zhang H, Damelin M, et al. Tumour-initiating cells: challenges and opportunities for anticancer drug discovery. Nat Rev Drug Discov. 2009;8:806–23.

    Article  CAS  Google Scholar 

  7. Reya T, Morrison SJ, Clarke MF, Weissman IL. Stem cells, cancer, and cancer stem cells. Nature. 2001;414:105–11.

    Article  CAS  Google Scholar 

  8. Ma S, Chan KW, Hu L, Lee TK, Wo JY, Ng IO, et al. Identification and characterization of tumorigenic liver cancer stem/progenitor cells. Gastroenterology. 2007;132:2542–56.

    Article  CAS  Google Scholar 

  9. Yamashita T, Honda M, Nakamoto Y, Baba M, Nio K, Hara Y, et al. Discrete nature of EpCAM+ and CD90+ cancer ste m cells in human hepatocellular carcinoma. Hepatology. 2013;57:1484–97.

    Article  CAS  Google Scholar 

  10. Yamashita T, Ji J, Budhu A, Forgues M, Yang W, Wang HY, et al. EpCAM-positive hepatocellular carcinoma cells are tumor-initiating cells with stem/progenitor cell features. Gastroenterology. 2009;136:1012–24.

    Article  CAS  Google Scholar 

  11. Xu X, Liu RF, Zhang X, Huang LY, Chen F, Fei QL, et al. DLK1 as a potential target against cancer stem/progenitor cells of hepatocellular carcinoma. Mol Cancer Ther. 2012;11:629–38.

    Article  CAS  Google Scholar 

  12. Chen Y, Yu D, Zhang H, et al. CD133+EpCAM+ Phenotype Possesses More Characteristics of Tumor Initiating Cells in Hepatocellular Carcinoma Huh7 Cells. Int J Biol Sci. 2012;8(7):992–1004.

    Article  CAS  Google Scholar 

  13. Ying LIU, Yang QI, Zhi-hui BAI, Chen-xu, et al. A novel matrine derivate inhibits differentiated human hepatoma cells and hepatic cancer stem-like cells by suppressing PI3K/AKT signaling pathways. Acta Pharmacol Sin. 2017;38:120–32.

    Article  Google Scholar 

  14. Zhou Y, et al. Aquaporin3 promotes the stem-like properties of gastric cancer cells via Wnt/GSK-3β/β-catenin pathway. Oncotarget. 2016;7(13):16529–41.

    Article  Google Scholar 

  15. Juuti Uusitalo K, et al. Aquapor in expression and function in human pluri potent stem cell-derived retinal pigment edepithelial cells. Invest Ophthalmol Vis Sci. 2013;54:3510–9.

    Article  Google Scholar 

  16. Yawei W, et al. Aquaporin 3 maintains the stemness of CD133+ hepatocellular carcinoma cells by activating STAT3. Cell Death Dis. 2019;10:465–80.

    Article  Google Scholar 

  17. Wang X, et al. AQP3 small interfering RNA and PLD2 small interfering RNA inhibit the proliferation and promote the apoptosisof squamous cell carcinoma. Mol Med Rep. 2017;16:1964–72.

    Article  CAS  Google Scholar 

  18. Huang X, Huang L, Shao M. Aquaporin 3 facilitates tumor growth in pancreatic cancer by modulating mTOR signaling. Biochem Biophys ResCommun. 2017;486:1097–102.

    Article  CAS  Google Scholar 

  19. Xiong G, et al. RNA interference influenced the proliferation and invasion of XWLC-05 lung cancer cells through inhibiting aquaporin3. Biochem Biophys Res Commun. 2017;485:627–34.

    Article  CAS  Google Scholar 

  20. Graziano ACE, Avola R, Pannuzzo G, Cardile V. Aquaporin1and3 modification as a result of chondrogenicdifferentiationofhumanmesenchymalstemcell. JCell Physiol. 2018;233:2279–91.

    Article  CAS  Google Scholar 

  21. Wu W, Baxter JE, Wattam SL, Hayward DG, Fardilha M, Knebel A, et al. Alternative splicing controls nuclear translocation of the cell cycle-regulated Nek2 kinase. J Biol Chem. 2007;282:26431–40.

    Article  CAS  Google Scholar 

  22. Liu X, Gao Y, Lu Y, Zhang J, Li L, Yin F. Up regulation of NEK2 is associated with drug resistance in ovarian cancer. Oncol Rep. 2014;3(1):745–54.

    Article  Google Scholar 

  23. Iwasaki H, Okabe T, Takara K, Toda T, Shimatani M, Oku H. Tumorselective cytotoxicity of benzo [c] phenanthridine derivatives from Toddaliaasiatica lam. Cancer Chemother Pharmacol. 2010;65:719–26.

    Article  CAS  Google Scholar 

  24. Varma MVS, Panchagnula R. Enhanced oral paclitaxel absorption with vitamin E TPGS: effect on solubility and permeability in vitro, in situ and in vivo. Eur J Pharm Sci. 2005;25:445–53.

    Article  CAS  Google Scholar 

  25. Collnot EM, Baldes C, Schaefer UF, Edgar KJ, Wempe MF, Lehr CM. Vitamin E TPGS p-glycoprotein inhibition mechanism: influence on conformational flexibility, intracellular ATP levels, and role of time and site of access. Mol Pharm. 2010;7:642–51.

    Article  CAS  Google Scholar 

  26. Li D, Liu S, Zhu J. Folic acid modified TPGS as a novel nanomicelle for delivery of nitidine chloride to improve apoptosis induction in Huh7 human hepatocellular carcinoma. BMC Pharmacol Toxicol. 2021;22:1–11.

    Article  Google Scholar 

  27. Yamashita T, Honda M, Nakamoto Y, Baba M, Nio K, Hara Y, et al. Discrete nature of EpCAM+ and CD90+ cancer stem cells in human hepatocellular carcinoma. Hepatology. 2013;57:1484–97.

    Article  CAS  Google Scholar 

  28. Chen J, et al. Aquaporin 3 promotes epithelial-mesenchymal transition in gastric cancer. J Exp Clin Cancer Res. 2014;33:38.

    Article  CAS  Google Scholar 

  29. Kang BW, et al. Expression of aquaporin-1, aquaporin-3, and aquaporin-5 correlates with nodal metastasis in colon cancer. Oncology. 2015;88:369–76.

    Article  CAS  Google Scholar 

  30. Li B, Jin L, Zhong K, Du D. Correlation of aquaporin 3 expression with the clinicopathologic characteristics of non-small cell lung cancer. Zhongguo Fei Ai Za Zhi. 2012;15:404–8.

    PubMed  Google Scholar 

  31. Gizachew YW, et al. Epigallocatechin gallate hinders human hepatoma and colon cancer sphere formation. J Gastroenterol Hepatol. 2016;31:256–64.

    Article  Google Scholar 

Download references


We are grateful to professor Bernard at Guangxi University for revising the manuscript.


This work was supported by the Guangxi Natural Science Foundation (2017GXNSFBA198021), Guangxi Key Laboratory of Zhuang and Yao Ethnic Medicine ((2014) No.32), Collaborative Innovation Center of Zhuang and Yao EthnicMedicine ((2013) No.20).

Author information

Authors and Affiliations



D. L. and H.Z. and T.L. and F.D. designed the main manuscript and D.L. and Q.Z. and Y.Z. prepared the experiments and prepared Figs. 1, 2, 3, 4, 5, 6 and 7. All authors reviewed the manuscript. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Danni Li.

Ethics declarations

Ethics approval and consent to participate

This study was approved by Ethics Committee of Guangxi University for Chinese medicine, all procedures reporting in this study on the animals were carried in accordance with the ARRIVE guidelines, and the study was carried out in accordance with the relevant guidelines and regulations. Huh 7 human hepatocellular carcinoma line and normal hepatocyte cell L-02 cells did not require ethics approval for their use. Informed consent was therefore not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, D., Zhang, Q., Zhou, Y. et al. A novel nitidine chloride nanoparticle overcomes the stemness of CD133+EPCAM+ Huh7 hepatocellular carcinoma cells for liver cancer therapy. BMC Pharmacol Toxicol 23, 48 (2022).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: