1,024
Views
6
CrossRef citations to date
0
Altmetric
Editorial: Cell Cycle Features

Anti-cancer drugs for cardioprotection

, &
Pages 155-156 | Received 06 Sep 2016, Accepted 23 Sep 2016, Published online: 10 Nov 2016
This article refers to:

Cardiovascular disease and cancer are the first and second common cause of death globally. An estimated 17.5 million people died from cardiovascular disease and 8.2 million died from cancer in 2012 according to the reports from World Health Organization (WHO). Although cardiovascular disease and cancer are regarded as 2 entirely different diseases before, recent studies suggest that these 2 diseases may share common risk factors, such as obesity, diabetes and chronic inflammation.Citation1 In addition, certain agents used for cancer therapies have been known to cause cardiotoxicity in the oncology patients. Thus, medications that have both anti-cancer and cardioprotective properties are urgently needed. Moreover, the potential biological mechanisms accounting for both diseases warrant more comprehensive study. To address this issue, we therefore thought of the potential application of certain anti-cancer agents on cardiovascular disease therapy.

Recent study from our group has revealed that an extract from medical mushroom Ganodermataceae, namely Ganoderma spore oil, exerts promising cardioprotective effects in both in vitro and in vivo models.Citation2 Ganoderma lucidum has been widely prescribed to cancer patient as a complementary treatment alongside chemo/radiotherapy in Asia. In this study, mice with heart failure modeling by transverse aortic constriction (TAC) were administered Ganoderma spore oil for 14 days. TAC mice with the Ganoderma treatment were found to have an elevated left ventriclular ejection fraction (LVEF) and left ventriclular fractional shortening (LVFS) as well as a reduced left ventricular end diastolic diameter (LVEDD) compared to mock treated TAC mice with vegetable oil. Moreover, Ganoderma spore oil administration also restored the cardiac output of TAC mice to the physiologic levels. These results indicated that Ganoderma is able to improve the cardiac function of TAC mice. Ganoderma lucidum is a genus of a well-studied traditional medical mushroom family Ganodermataceae, which contains a number of bioactive components including polysaccharides, ganoderic acid (triterpene) and adenosine. Ganoderma lucidum and another member of the Ganodermataceae family, Amauroderma rude, are well-known for their anti-cancer activities which include inhibiting cell proliferation and inducing cell apoptosis.Citation3,4 Ergosterol peroxide, purified from Ganoderma lucidum, has been found to effectively induce cancer cell death and suppress cell migration, cell cycle progression and colony formation in human hepatocellular carcinoma cells.Citation3 Meanwhile, ergosterol purified from Amauroderma rude is able to accelerate cell apoptosis in breast cancer, and suppress malignant cell behaviors, such as cancer cell migration, invasion and colony formation.Citation4 In several animal models, ergosterol was validated to prolong survival of the mice injected with murine melanoma cell line,Citation4 activate immune cell activity and inhibit tumor growth of the mice injected with murine breast cancer cell line.Citation5 It was confirmed in our recent findings that these medical components used for inhibiting cancer growth can improve cardiac function. Our results suggest that certain anti-cancer agents have the potential to be clinically employed as cardioprotective agents.

With respect to the fact that Ganoderma lucidum has dual therapeutic effects of anti-cancer and cardioprotection, we hypothesized that such effects might be mediated via shared biological mechanisms of these 2 diseases. Non-coding RNAs might be the fascinating candidates, which serve as key mediators for Ganoderma lucidum against both cancer and heart failure. The microRNA and circular RNA are 2 of the major types of non-coding RNAs. Our previous study unraveled that ergosterol peroxide isolated from Ganoderma lucidum induced cell death by abolishing microRNA miR-378-mediated tumor cells on chemoresistance.Citation6 In addition to microRNAs, our recent study also validated that the cardioprotective effect of Ganoderma lucidum is mediated by a circular RNA circ-Foxo3 encoded by the Foxo3 gene.Citation2 Increased expression of circ-Foxo3 RNA has also been found in mice with reduced cardiac function.Citation7 In an in vitro study, Ganoderma spore oil treatment significantly reduced the level of circ-Foxo3 in mouse cardiac fibroblasts subjected to H2O2-induced oxidative stress. In line with the in vitro findings, the circ-Foxo3 levels were also found to be significantly decreased in the heart tissues of TAC mice after Ganoderma spore oil administration compared to mock group.Citation2 Collectively, the above results from our group suggest that microRNA and circular RNA, especially circ-Foxo3, may play an important role in mediating both anti-cancer and cardioprotective effect of Ganoderma.

In the past decades, non-coding RNAs gained extensive attention due to their diverse roles in a variety of diseases. Especially, research interest toward circular RNA is growing since there is increasing evidence of their roles in gene regulation and disease progression. The acknowledgment that circular RNAs play dual roles against both cancer and cardiovascular disease will raise a new perspective to further understand the shared mechanisms of the progression between these 2 diseases. Our pre-clinic study also provides an implication of using non-chemotherapy anti-cancer medication to protect cardiac function. Ultimately, this may benefit the patients suffering from cardiovascular toxicity due to chemotherapy.

Disclosure of potential conflicts of interest

No potential conflicts of interest were disclosed.

Funding

Our studies were supported by The High-Level Leading Talent Introduction Program of GDAS (2016GDASRC-0102), The Introduction of Leading Talent Project of Guangdong Province, and Guangdong Key Technology Program (2012A020100010).

References

  • Koene RJ, Prizment AE, Blaes A, Konety SH. Shared risk factors in cardiovascular disease and cancer. Circulation 2016; 133:1104-14; PMID:26976915; http://dx.doi.org/10.1161/CIRCULATIONAHA.115.020406
  • Xie YZ, Yang F, Tan W, Li X, Jiao C, Huang R, Yang BB. The anti-cancer components of Ganoderma lucidum possesses cardiovascular protective effect by regulating circular RNA expression. Oncoscience 2016; 3:203–207; PMID:27713910; http://dx.doi.org/10.18632/oncoscience.316
  • Li X, Wu Q, Bu M, Hu L, Du WW, Jiao C, Pan H, Sdiri M, Wu N, Xie Y, et al. Ergosterol peroxide activates Foxo3a-mediated cell death signaling by inhibiting AKT and c-Myc in human hepatocellular carcinoma cells. Oncotarget 2016; 7:33948–33959; PMID:27058618; http://dx.doi.org/10.18632/oncotarget.8608
  • Li X, Wu Q, Xie Y, Ding Y, Du WW, Sdiri M, Yang BB. Ergosterol purified from medicinal mushroom Amauroderma rude inhibits cancer growth in vitro and in vivo by up-regulating multiple tumor suppressors. Oncotarget 2015; 6:17832-46; PMID:26098777; http://dx.doi.org/10.18632/oncotarget.4026
  • Pan H, Han Y, Huang J, Yu X, Jiao C, Yang X, Dhaliwal P, Xie Y, Yang BB. Purification and identification of a polysaccharide from medicinal mushroom Amauroderma rude with immunomodulatory activity and inhibitory effect on tumor growth. Oncotarget 2013; 6:17777-91; http://dx.doi.org/10.18632/oncotarget.4397
  • Wu QP, Xie YZ, Deng Z, Li XM, Yang W, Jiao CW, Fang L, Li SZ, Pan HH, Yee AJ, et al. Ergosterol peroxide isolated from Ganoderma lucidum abolishes microRNA miR-378-mediated tumor cells on chemoresistance. PLoS One 2012; 7:e44579; PMID:22952996; http://dx.doi.org/10.1371/journal.pone.0044579
  • Du WW, Yang W, Chen Y, Wu ZK, Foster FS, Yang Z, Li X, Yang BB. Foxo3 circular RNA promotes cardiac senescence by modulating multiple factors associated with stress and senescence responses. Eur Heart J 2016; in press; PMID:26873092; http://dx.doi.org/10.1093/eurheartj/ehw001

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.