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Oncotarget. 2017 January 17; 8(3): 4837–4848.
Published online 2016 November 25. doi:  10.18632/oncotarget.13596
PMCID: PMC5341749

Astragalus polysaccharide restores autophagic flux and improves cardiomyocyte function in doxorubicin-induced cardiotoxicity

Abstract

Doxorubicin (adriamycin), an anthracycline antibiotic, is commonly used to treat many types of solid and hematological malignancies. Unfortunately, clinical usage of doxorubicin is limited due to the associated acute and chronic cardiotoxicity. Previous studies demonstrated that Astragalus polysaccharide (APS), the extracts of Astragalus membranaceus, had strong anti-tumor activities and anti-inflammatory effects. However, whether APS could mitigate chemotherapy-induced cardiotoxicity is unclear thus far. We used a doxorubicin-induced neonatal rat cardiomyocyte injury model and a mouse heart failure model to explore the function of APS. GFP-LC3 adenovirus-mediated autophagic vesicle assays, GFP and RFP tandemly tagged LC3 (tfLC3) assays and Western blot analyses were performed to analyze the cell function and cell signaling changes following APS treatment in cardiomyocytes. First, doxorubicin treatment led to C57BL/6J mouse heart failure and increased cardiomyocyte apoptosis, with a disturbed cell autophagic flux. Second, APS restored autophagy in doxorubicin-treated primary neonatal rat ventricular myocytes and in the doxorubicin-induced heart failure mouse model. Third, APS attenuated doxorubicin-induced heart injury by regulating the AMPK/mTOR pathway. The mTOR inhibitor rapamycin significantly abrogated the protective effect of APS. These results suggest that doxorubicin could induce heart failure by disturbing cardiomyocyte autophagic flux, which may cause excessive cell apoptosis. APS could restore normal autophagic flux, ameliorating doxorubicin-induced cardiotoxicity by regulating the AMPK/mTOR pathway.

Keywords: astragalus polysaccharide, doxorubicin, cardiomyocyte, autophagy, AMPK/mTOR

INTRODUCTION

Doxorubicin (DOX) is widely used as a broad-spectrum anticancer chemotherapeutic drug. Treatment with this drug results in generation of reaction oxygen species (ROS), DNA mutagenesis, inhibition of protein synthesis, cell membrane damage, and cell apoptosis [1]. Although DOX is beneficial as a cancer therapeutic medicine, it is also associated with acute and chronic cardiotoxicity, which leads to cardiomyopathy and congestive heart failure [24]. Elucidating the mechanism underlying DOX-induced cardiotoxicity may identify strategies to reduce cardiomyopathy risks for cancer patients.

Previous studies suggested that free radical-induced mitochondrial damage due to elevated ROS production is the major contributing factor to doxorubicin-induced cardiotoxicity, but recent reports have demonstrated that ROS scavengers failed to prevent heart failure [5, 6]. Therefore, there must be another mechanism regulating doxorubicin-induced cardiotoxicity. Typically, cardiotoxicity is attributed to cardiomyocyte loss through apoptosis and/or necrosis [7, 8]. However, recent evidence suggests that dysregulation of autophagy may also contribute to cardiomyocyte loss, causing heart failure [9].

Autophagy is an important cytoplasmic quality control system that removes protein aggregates and damaged organelles [1516]. In physiological conditions, autophagy sustains optimal cardiomyocyte conditions by degrading or recycling misfolded proteins and damaged organelles [1012]. Autophagic dysfunction may result in accumulation of misfolded/damaged proteins, inadvertently disrupting cardiac homeostasis. Alterations in autophagic homeostasis have been observed in various heart pathological conditions, such as oxidative stress or ischemia reperfusion [1315]. However, the role of autophagy in doxorubicin-induced cardiomyopathy still remains poorly defined.

Astragalus species derived from the dry roots of Astragalus membranaceus [16] have been widely used in traditional Chinese medicine as an antiperspirant, antihypertensive, diuretic, and tonic treatments [1719]. Astragalus polysaccharide (APS), the extracts of Astragalus membranaceus, also has strong anti-tumor and anti-glomerulonephritis activities [20, 21] and alleviates arterial inflammation [22]. APS has been shown to ameliorate the side effects of chemotherapeutic drugs in cancer patients. In a previous study, APS suppressed oxidative stress and apoptosis by regulating the PI3k/Akt and p38MAPK pathways [23].

In this study, we investigated the protective effects of APS in doxorubicin-induced cardiotoxicity, and provided novel insight into how APS regulate cardiomyocyte autophagy in vivo and in vitro. Our results revealed that APS could restore normal autophagic flux and improve heart function by regulating AMPK/mTOR pathway in doxorubicin-induced cardiotoxicity. These findings provide insight into the mechanisms of doxorubicin-induced cardiotoxicity in cancer patients and a new potential treatment for the side effects of doxorubicin.

RESULTS

Doxorubicin disturbs cardiomyocyte autophagic flux

Our previous study revealed that doxorubicin treatment significantly reduced cell viability in a dose-dependent manner compared with the control, as shown by the cell viability assay [23]. To determine whether autophagy is involved in doxorubicin-induced cardiotoxicity, several important signaling pathway proteins were measured. The active (cleaved) caspase-3 (c-caspase-3) was significantly increased in a concentration-dependent manner in NRVMs treated with doxorubicin for 24 h, indicating elevated apoptosis (Figure (Figure1A).1A). Additionally, the level of LC3B II/I was significantly increased in 0.1 μM-0.5 μM doxorubicin treatment group, and was subsequently decreased in the 1 μM-5 μM doxorubicin-treated NRVMs (Figure (Figure1A).1A). So the cell viability decline might result from autophagy more than apoptosis in the treatment of 0.5μM doxorubicin. Therefore, 0.5 μM doxorubicin was chosen to establish the in vitro doxorubicin-induced cardiotoxicity model.

Figure 1
Doxorubicin induces cardiotoxicity by disturbing normal autophagy in cardiomyocytes

To determine whether doxorubicin-induced accumulation of LC3-II is caused by enhanced autophagic flux or impaired degradation, GFP-LC3 adenovirus, which indicates the formation of autophagosomes, was transduced into NRVMs. After the doxorubicin treatment, GFP signals were significantly elevated in NRVMs, indicating increased formation of autophagosomes (Figure (Figure1B).1B). Additionally, a marker for autophagic flux P62/SQSTM1, which is a polyubiquitin-binding protein that is degraded by autophagy and inversely related to autophagy during normal flux, was assessed by Western blot. We found that p62/SQSTM1 was significantly elevated in the NRVMs treated with doxorubicin, indicating an inability to complete autophagy (Figure (Figure1A1A).

To assess autophagic flux, H9c2 cells were transiently transfected with a plasmid harboring a tandem fluorescent mRFP-GFP-LC3 (tfLC3) (Figure (Figure1C).1C). The GFP signal represents the autophagosomes, and the RFP signal represents the normal maturation of autophagosomes into autolysosomes. However, the GFP signal is not present in the acid environment of autolysosomes. Therefore, if most puncta exhibit both red and green signals, it indicates that autophagy is impaired at some steps. Under the dosage of 0.5 μM doxorubicin treatment, most of the red puncta were colocalized with green puncta (shown by the yellow signal in merged photos), indicating an impairment of autophagic flux. Together, the data suggested that the excess autophagy might be due to enhanced autophagosome formation as well as impaired autophagic flux.

APS restores autophagy in doxorubicin-treated primary neonatal rat ventricular myocytes

In the presence of 50 μg/ml APS, autophagosome formation in cardiomyocytes was reduced compared with the 0.5 μM doxorubicin-treated group, as shown by the GFP-LC3B adenovirus assays (Figure (Figure2A).2A). As shown in Figure Figure2B,2B, pretreatment with APS reversed the autophagic flux induced by doxorubicin, as shown by decreased co-localization of the tandem RFP-GFP-LC3 plasmid in merged images, which indicated that APS could attenuate doxorubicin-induced impaired autophagosome degradation. To further examine APS involvement in regulating autophagosome degradation, bafilomycin (BFA) was administered to block autophagic flux in cardiomyocytes. BFA is a classical inhibitor of the fusion of autophagosomes to lysosomes, which abolishes autophagosome degradation. As shown in Figure Figure2C,2C, without BFA, the doxorubicin-induced LC3BII/I increase was alleviated by APS; following administration of BFA, which blocked the degradation of autophagosomes, LC3BII/I was still significantly increased in the doxorubicin group compared with the control. These data further confirmed that doxorubicin increased the formation of autophagosomes. However, compared with the doxorubicin group, APS treatment did not further decrease LC3B II/I. Therefore, we hypothesized that APS also played a role in restoring autophagosome degradation. Taken together, APS normalized autophagic flux by suppressing autophagosome formation and enhancing autophagosome degradation.

Figure 2
APS restores autophagy in doxorubicin-treated cardiomyocytes

Moreover, as shown in Figure Figure3A,3A, treatment with 50 μg/ml APS reversed the doxorubicin-induced increase in LC3B II/I and p62/SQSTM1. And caspase-3 activation was apparently suppressed by 50 μg/ml APS. These results indicate that excessive autophagy induced by doxorubicin promotes cardiomyocyte apoptosis (Figure (Figure3A),3A), while APS could potentially restore doxorubicin-induced excess accumulation of autophagosomes in cultured NRVMs. To confirm that APS could protect cardiomyocytes by attenuating LC3B activation, rapamycin (mTOR inhibitor), a classical autophagy activator, was used in cardiomyocyte. Pretreatment with 100 nM rapamycin effectively reversed the protective effect of APS in cardiomyocytes (Figure (Figure3B).3B). Activated caspase-3 was elevated in the APS protective group with pretreatment of rapamycin.

Figure 3
The protective role of APS in doxorubicin-induced cardiomyocyte injury

APS ameliorates doxorubicin-induced heart failure by restoring normal autophagy and decreasing apoptosis in vivo

After verifying the protective effect of APS in vitro, we then determined whether APS could preserve heart function in vivo. We generated a heart failure model using doxorubicin-treated C57BL/6 male mice. The body weight and heart weight/tibia length ratio decreased significantly after doxorubicin treatment for 5 days. Pretreatment with APS could significantly increase mouse body weight and heart weight/tibia length ratio (Figure (Figure4A).4A). Echocardiographic M-mode tracings and measurements were used to analyze heart function. Compared with sham mice, doxorubicin-treated mice exhibited decreased heart function as measured by the ejection fraction (EF%) and shortening index (FS%). APS treatment improved mouse heart function compared with that of doxorubicin treated mice. (Figure 4B-4C). As shown by H&E staining, doxorubicin-induced heart failure was associated with cardiac tissue disorder (Figure (Figure4D).4D). The cell apoptotic rate increased from 1.33±1.05% (Sham) to 22.28±8.39% (DOX) as demonstrated by TUNEL staining. Importantly, pretreatment with APS attenuated doxorubicin-induced cardiomyocyte apoptosis (11.53±3.54%) (Figure (Figure4E).4E). Western blot analysis also showed that APS suppressed doxorubicin-induced LC3B II/I and caspase-3 activation and promote Bcl-2 protein expression in vivo (Figure (Figure4F4F).

Figure 4
APS ameliorates doxorubicin-induced heart failure by restoring normal autophagy and decreasing apoptosis in vivo

APS attenuates doxorubicin-induced heart injury by regulating the AMPK/mTOR pathway

To further explore the protective effects of APS on doxorubicin-induced heart injury, autophagy-related signaling pathways were analyzed in response to doxorubicin treatment and APS pretreatment. The AMPK-dependent mTOR was determined to be responsible for the suppression of autophagy after APS pretreatment. According to the Western blot results, 0.5 μM doxorubicin treatment led to a significant decrease in mTOR phosphorylation, which in turn activated autophagy (Figure (Figure5A).5A). Interestingly, we found that AMPK, a vital regulator of the energy response and activator of mTOR, was substantially increased after doxorubicin treatment, and APS could inhibit its activation (Figure (Figure5A).5A). Similar results were obtained in the doxorubicin-induced heart failure mouse model (Figure (Figure5B).5B). Next, rapamycin was used to determine whether AMPK/mTOR regulates the protective role of APS in doxorubicin-induced cardiotoxicity. As shown in the Figure Figure5C,5C, rapamycin significantly suppressed APS induced mTOR phosphorylation and reverse the protective effect. Taken together, these data suggest that APS could significantly restore autophagic flux and promote cell survival, which could be abrogated by the mTOR inhibitor rapamycin.

Figure 5
APS attenuates doxorubicin-induced heart injury by regulation of the phosphorylation of AMPK/mTOR

DISCUSSION

Clinical use of doxorubicin as an effective anticancer chemotherapeutic agent for the treatment of solid tumors and hematologic malignancies is limited due to acute and chronic cardiotoxicity. In vitro and in vivo experiments have determined that doxorubicin could induce cardiomyocyte loss and heart dysfunction in a dose-dependent manner [24], which was confirmed by our study. However, the underlying mechanisms of doxorubicin cardiotoxicity are still unclear. Apoptosis induced by caspase-9/caspase-3 pathway activation and necrosis are believed to be involved in cardiomyocyte loss caused by a large dose of doxorubicin. However, high doses of doxorubicin are unrealistic, given current clinical use. Therefore, determining the role of autophagy under a low dose treatment is important to decrease its possible side effects.

Autophagy is an important cellular process that responds to various internal and external nutrients, but abnormal autophagy may cause multiple diseases, including cardiovascular diseases. Based on recent findings, it is highly possible that autophagy also acts as an important regulator in the pathogenesis of heart failure caused by doxorubicin treatment. In the present study, cell viability was significantly decreased in doxorubicin-treated cardiomyocytes and mice, with a concomitant significant elevation of LC3B II/I. To determine the effect of doxorubicin-induced cardiotoxicity on autophagy, we detected the autophagic flux in cardiomyocytes. According to a previous study, doxorubicin could impair the normal degradation of autophagosomes and halt autophagy [25]. In our study, we found that doxorubicin increased the formation of autophagosomes and blocked normal autophagic flux, which led to excessive accumulation of autophagosomes and autophagic cell death. Thus, autophagic death might play an important role in the cardiotoxicity caused by doxorubicin.

APS is a potent traditional medicine has been used to inhibit tumor growth, enhance immunity, and potently alleviate arterial inflammation [26, 27]. Several previous studies demonstrated that APS may be an effective treatment for heart diseases, such as myocardial hypertrophy and heart failure. Many clinical studies also indicated that APS could mitigate the side effects of chemotherapeutic drugs [17]. However, whether APS could protect cardiomyocyte from doxorubicin-induced cardiotoxicity was still not clear. In the present study, we found that APS significantly reduced doxorubicin-induced cardiomyocyte injury by restoring autophagic flux and autophagosome formation.

Previous studies revealed that doxorubicin treatment reduced the activation of mammalian target of rapamycin (mTOR) [2830]. Interestingly, we found that APS treatment could dramatically decrease AMPK activation and promote mTOR activation. We hypothesized that AMPK/mTOR may be one of the key pathways in the protective effects of APS. Rapamycin is a classic reagent that induces autophagy by suppressing the phosphorylation of mTOR. According to our results, rapamycin could significantly reverse the protective effects of APS. Therefore, the data indicated APS could protect cardiomyocytes from doxorubicin-induced cardiotoxicity by suppressing phosphorylated AMPK, a negative regulator of mTOR phosphorylation, in turn reducing the level of autophagy.

In this study, pretreatment with APS could restore normal autophagic flux in doxorubicin-induced cardiotoxicity and improve heart function. These results suggest that APS may be a novel drug for the treatment of doxorubicin-induced cardiotoxicity.

There are several important issues that must be investigated before these findings can be applied to the clinic. Further studies are needed to assess the safety, efficacy and clinical application of APS. Second, APS affects various pathways; therefore, our study that focused only on its anti-autophagic properties is limited. Third, whether doxorubicin induces DNA damage should be determined. Therefore, p53 might be also involved in the doxorubicin-induced cardiotoxicity. Zhu et al (34) showed that acute doxorubicin cardiotoxicity is associated with p53-induced inhibition of mTOR. Thus, APS may not only inhibit AMPK activation but also regulate other upstream regulators to regulate mTOR and protect cardiomyocyte. Further studies are required to define the potential protective roles of APS in doxorubicin-induced cardiotoxicity.

In summary, our findings demonstrated that doxorubicin could induce cardiotoxicity by disturbing autophagic flux, which lead to excessive cell apoptosis. APS could restore normal autophagic flux, and ameliorate doxorubicin-induced cardiotoxicity by regulating the AMPK/mTOR pathway.

MATERIALS AND METHODS

Reagents

Antibodies against p62, Beclin1, ERK1/2, phosphorylated-ERK1/2, AMPK, phosphorylated-AMPK, mTOR, phosphorylated-mTOR, Bcl-2 and caspase-3 were purchased from Cell Signaling Technology (Danvers, MA, USA); GAPDH antibody was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA); LC3B antibody was purchased from Sigma (St. Louis, MO, USA). Secondary antibodies directed against rabbit or goat were purchased from Cell Signaling Technology. Unless otherwise indicated, all chemicals were purchased from Sigma or Amresco.

Preparation of APS

APS was purchased from the Shifeng Biological Co., Shanghai, China. APS was dissolved in PBS to generate a 10 mg/ml working solution and then diluted with DMEM culture medium at different concentrations for the following experimental treatments.

Animals

Specific pathogen Free (SPF) male C57BL/6 mice (8 weeks old) were purchased from Beijing Vital River Laboratories and housed in SPF facilities. The mice were separated into three groups: sham, doxorubicin-treated, and doxorubicin-treated mice with APS. Sham mice were injected and orally administered saline solution. The doxorubicin-treated mice (DOX) were intraperitoneal injected with 20 mg/kg doxorubicin and orally administered APS or an equivalent volume of saline. The APS treatment group (DOX+APS) was pretreated with APS (1.5 g/kg/day) for 3 days by gavage, and this group was then intraperitoneal injected with 20 mg/kg doxorubicin. The APS treatment was continued for 3 days after doxorubicin injection [4, 23]. All the mice were euthanized 5 days after the initial injection of doxorubicin. All animal experiments conformed to the protocols approved by Animal Use and Care Committee of Beijing Hospital and the Guide for Care and Use of Laboratory Animals (NIH Publication #85-23, revised 1996).

Echocardiography

Echocardiography was performed using Vevo 770 and Vevo 2100 (VisualSonics) instruments from Anzhen Hospital. According to the protocol, mice were lightly anesthetized with 1-1.5% isofluorane in oxygen until the heart rate stabilized to 400 to 500 beats per minute before echocardiography. Ejection fraction (EF)% and fraction shortening (FS)% were calculated with Vevo Analysis software as previously described [31].

Histology

Tissues were processed by paraffin sectioning, and H&E staining was performed on the sections according to the manufacturer's protocol (Sigma-Aldrich).

Terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) and Hoechst 33342 staining of heart cryosections

Nuclear fragmentation was detected by TUNEL staining (Roche) and 10 mM Hoechst 33342 as previously described [23]. Cells in 10 randomly chosen fields from each dish were counted to semi-quantitatively determine the ratio of apoptotic nuclei. Each data point indicates results from 1600 to 2000 cells in 4 independent experiments [23].

Isolation and culture of rat cardiomyocytes

Neonatal rat ventricular myocytes (NRVMs) were isolated from 1–3-day-old Sprague-Dawley rats using a combined trypsin and collagenase type II digestion method as previously described [23]. The cardiomyocytes were plated at a density of 6.6 × 104 cells/cm2 in DMEM supplemented with 10% FBS and selected using 0.1 mM 5-bromo-2-deoxyuridine.

Western blot analysis

Cell lysates were analyzed by 12% SDS-PAGE and transferred to PVDF membranes by wet transfer. The membranes were blocked with 5% milk for 1 h in room temperature and incubated with specific first antibodies (1:1000) overnight at 4°C. The primary antibodies were thoroughly washed with 5 washes of TBST (TBS containing 0.1% Tween 20), 10 min each; then, the membranes were incubated with horseradish peroxidase–conjugated secondary antibodies (1:3000) in TBST for 1 h at room temperature. Protein expression was then detected by ECL. Densitometry analysis was then performed with ImageJ software.

GFP-LC3 adenovirus preparation and adenoviral transduction

The adenovirus GFP-LC3 was purchased from Hanbio Company of China. The cardiomyocytes were transfected with 30 M.O.I. of GFP-LC3 adenovirus for 24 h and then treated with DOX or DOX+APS for 24 h. The labeled autophagic vesicles were measured using ImageJ software and are shown as a percentage of the total number of GFP-LC3 dots.

GFP and RFP tandemly tagged LC3 (tfLC3) assay

The method to evaluate tandem fluorescent LC3 puncta using the mRFP-GFP-LC3 plasmid was previously described [32]. H9c2 cells cultured on cover slips were transduced with the mRFP-GFP-LC3 plasmid for 24 h and then treated with DOX or DOX+APS for another 24 h. Then, the cells were viewed with an inverted fluorescence microscope. If there was a significant population of red-only signals, then the autophagosomes normally matured into autolysosomes (where the GFP is relatively unstable). If most puncta exhibited both red and green signals, autophagy was impaired at some step. Co-localization efficiency of mRFP with GFP signals of tfLC3 puncta was measured using ImageJ software and shown as the percentage of the total number of mRFP puncta.

Statistical analysis

The data are expressed as the mean ± SEM. Student's t-test was used to compare two conditions, and one-way ANOVA with Bonferroni correction was used for multiple comparisons. Probability values less than 0.05 were considered significant.

Abbreviations

AMPK
AMP-activated protein kinase
mTOR
mammalian target of rapamycin
TUNEL
terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling
FBS
fetal bovine serum
PBS
phosphate buffered saline
GAPDH
glyceraldehyde-3-phosphate dehydrogenase
H&E
hematoxylin and eosin
PI3K
phosphoinositide-3-kinase
ERK
extracellular signal-regulated kinase.

Footnotes

CONFLICTS OF INTEREST

The authors declare no conflict of interest.

FUNDINGS

This work is supported by grants from the National Basic Research Program of China (2012CB517502, 2014CB910503), the National Natural Science Foundation of China (81470427, 81200221, 81570789, 81270887, 81270854, 81270948, 81471071), and the Beijing Hospital Nova project (BJ-2016-045).

Contributed by

Author contributions

Conceived and designed the experiments: YC, TS and JL. Performed the experiments: YC, TS, XH, YL, YR and QW. Analyzed the data: YC, TS and QW. Contributed reagents/materials/analysis tools: BC, JP, GL, CD, YM and SW. Wrote the paper: YC, TS, SZ and JL.

REFERENCES

1. Lal S, Mahajan A, Chen WN, et al. Pharmacogenetics of target genes across doxorubicin disposition pathway: a review. Curr Drug Metab. 2010;11:115–128. [PubMed]
2. Smith LA, Cornelius VR, Plummer CJ, et al. Cardiotoxicity of anthracycline agents for the treatment of cancer: systematic review and meta-analysis of randomised controlled trials. BMC Cancer. 2010;10:337. [PMC free article] [PubMed]
3. Takemura G, Fujiwara H. Doxorubicin-induced cardiomyopathy from the cardiotoxic mechanisms to management. Prog Cardiovasc Dis. 2007;49:330–352. [PubMed]
4. Ruan Y, Dong C, Patel J, et al. SIRT1 suppresses doxorubicin-induced cardiotoxicity by regulating the oxidative stress and p38MAPK pathways. Cell Physiol Biochem. 2015;35:1116–1124. [PubMed]
5. Tacar O, Dass CR. Doxorubicin-induced death in tumour cells and cardiomyocytes: is autophagy the key to improving future clinical outcomes? J Pharm Pharmacol. 2013;65:1577–1589. [PubMed]
6. Zhang S, Liu X, Bawa-Khalfe T, et al. Identification of the molecular basis of doxorubicin-induced cardiotoxicity. Nat Med. 2012;18:1639–1642. [PubMed]
7. Hein S, Arnon E, Kostin S, et al. Progression from compensated hypertrophy to failure in the pressure-overloaded human heart: structural deterioration and compensatory mechanisms. Circulation. 2003;107:984–991. [PubMed]
8. Gottlieb RA, Finley KD, Mentzer RM., Jr Cardioprotection requires taking out the trash. Basic Res Cardiol. 2009;104:169–180. [PMC free article] [PubMed]
9. Goswami SK, Das DK. Autophagy in the myocardium: Dying for survival? Exp Clin Cardiol. 2006;11:183–188. [PMC free article] [PubMed]
10. Luo H, Wong J, Wong B. Protein degradation systems in viral myocarditis leading to dilated cardiomyopathy. Cardiovasc Res. 2010;85:347–356. [PubMed]
11. Naiki H, Nagai Y. Molecular pathogenesis of protein misfolding diseases: pathological molecular environments versus quality control systems against misfolded proteins. J Biochem. 2009;146:751–756. [PubMed]
12. Gottlieb RA, Mentzer RM. Autophagy during cardiac stress: joys and frustrations of autophagy. Annu Rev Physiol. 2010;72:45–59. [PMC free article] [PubMed]
13. Hariharan N, Zhai P, Sadoshima J. Oxidative stress stimulates autophagic flux during ischemia/reperfusion. Antioxid Redox Signal. 2011;14:2179–2190. [PMC free article] [PubMed]
14. Takagi H, Matsui Y, Sadoshima J. The role of autophagy in mediating cell survival and death during ischemia and reperfusion in the heart. Antioxid Redox Signal. 2007;9:1373–1381. [PubMed]
15. Gurusamy N, Das DK. Autophagy, redox signaling, and ventricular remodeling. Antioxid Redox Signal. 2009;11:1975–1988. [PMC free article] [PubMed]
16. Zhang Y, Shi P, Yao H, et al. Metabolite profiling and pharmacokinetics of herbal compounds following oral administration of a cardiovascular multi-herb medicine (Qishen yiqi pills) in rats. Curr Drug Metab. 2012;13:510–523. [PubMed]
17. Liu W, Gao FF, Li Q, et al. Protective effect of astragalus polysaccharides on liver injury induced by several different chemotherapeutics in mice. Asian Pac J Cancer Prev. 2014;15:10413–10420. [PubMed]
18. Chen W, Li Y, Yu M. Astragalus polysaccharides: an effective treatment for diabetes prevention in NOD mice. Exp Clin Endocrinol Diabetes. 2008;116:468–474. [PubMed]
19. Chen W, Lai Y, Wang L, et al. Astragalus polysaccharides repress myocardial lipotoxicity in a PPARalpha-dependent manner in vitro and in vivo in mice. J Diabetes Complications. 2015;29:164–175. [PubMed]
20. Li S, Zhang Y, Zhao J. Preparation and suppressive effect of astragalus polysaccharide in glomerulonephritis rats. Int Immunopharmacol. 2007;7:23–28. [PubMed]
21. Guo L, Bai SP, Zhao L, et al. Astragalus polysaccharide injection integrated with vinorelbine and cisplatin for patients with advanced non-small cell lung cancer: effects on quality of life and survival. Med Oncol. 2012;29:1656–1662. [PubMed]
22. Zhu YP, Shen T, Lin YJ, et al. Astragalus polysaccharides suppress ICAM-1 and VCAM-1 expression in TNF-alpha-treated human vascular endothelial cells by blocking NF-kappaB activation. Acta Pharmacol Sin. 2013;34:1036–1042. [PMC free article] [PubMed]
23. Cao Y, Ruan Y, Shen T, et al. Astragalus polysaccharide suppresses doxorubicin-induced cardiotoxicity by regulating the PI3k/Akt and p38MAPK pathways. Oxid Med Cell Longev. 2014;2014:674219. [PMC free article] [PubMed]
24. Nitiss KC, Nitiss JL. Twisting and ironing: doxorubicin cardiotoxicity by mitochondrial DNA damage. Clin Cancer Res. 2014;20:4737–4739. [PMC free article] [PubMed]
25. Kawaguchi T, Takemura G, Kanamori H, et al. Prior starvation mitigates acute doxorubicin cardiotoxicity through restoration of autophagy in affected cardiomyocytes. Cardiovasc Res. 2012;96:456–465. [PubMed]
26. Liu QY, Yao YM, Zhang SW, et al. Astragalus polysaccharides regulate T cell-mediated immunity via CD11c(high)CD45RB(low) DCs in vitro. J Ethnopharmacol. 2011;136:457–464. [PubMed]
27. Li J, Bao Y, Lam W, et al. Immunoregulatory and anti-tumor effects of polysaccharopeptide and Astragalus polysaccharides on tumor-bearing mice. Immunopharmacol Immunotoxicol. 2008;30:771–782. [PubMed]
28. Dai W, Yang F, Ma L, et al. Combined mTOR inhibitor rapamycin and doxorubicin-loaded cyclic octapeptide modified liposomes for targeting integrin alpha3 in triple-negative breast cancer. Biomaterials. 2014;35:5347–5358. [PubMed]
29. Numakura K, Tsuchiya N, Akihama S, et al. Successful mammalian target of rapamycin inhibitor maintenance therapy following induction chemotherapy with gemcitabine and doxorubicin for metastatic sarcomatoid renal cell carcinoma. Oncol Lett. 2014;8:464–466. [PMC free article] [PubMed]
30. Sishi BJ, Loos B, van RJ, et al. Autophagy upregulation promotes survival and attenuates doxorubicin-induced cardiotoxicity. Biochem Pharmacol. 2013;85:124–134. [PubMed]
31. Shen T, Aneas I, Sakabe N, et al. Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function. J Clin Invest. 2011;121:4640–4654. [PMC free article] [PubMed]
32. Kimura S, Noda T, Yoshimori T. Dissection of the autophagosome maturation process by a novel reporter protein, tandem fluorescent-tagged LC3. Autophagy. 2007;3:452–460. [PubMed]

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