1. Tanshinone Suppresses Arecoline-Induced EpithelialMesenchymal Transition in Oral Submucous Fibrosis by Epigenetically Reactivating the p53 Pathway
    Lian Zheng et al, 2018, Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics CrossRef
  2. Sodium Danshensu Inhibits Oral Cancer Cell Migration and Invasion by Modulating p38 Signaling Pathway
    V. Bharath Kumar et al, 2020, Frontiers in Endocrinology CrossRef
  3. Tanshinone IIA sensitizes TRAIL-induced apoptosis in glioblastoma through inducing the expression of death receptors (and suppressing STAT3 activation)
    Xiaokun Zhou et al, 2021, Brain Research CrossRef
  4. Pharmacological basis of tanshinone and new insights into tanshinone as a multitarget natural product for multifaceted diseases
    Zhibei Li et al, 2020, Biomedicine & Pharmacotherapy CrossRef
  5. Diterpenes and Their Derivatives as Potential Anticancer Agents
    Muhammad Torequl Islam, 2017, Phytotherapy Research CrossRef
  6. Tanshinone IIA: A Review of its Anticancer Effects
    Zhong‐ying Fang et al, 2021, Frontiers in Pharmacology CrossRef
  7. Phosphoproteome Analysis Reveals Dynamic Heat Shock Protein 27 Phosphorylation in Tanshinone IIA-Induced Cell Death
    Chieh-Fan Yin et al, 2020, Journal of Proteome Research CrossRef
  8. Tanshinone IIA Inhibits Epithelial-Mesenchymal Transition in Bladder Cancer Cells via Modulation of STAT3-CCL2 Signaling
    Sung-Ying Huang et al, 2017, International Journal of Molecular Sciences CrossRef
  9. An overview of the anti-cancer actions of Tanshinones, derived from Salvia miltiorrhiza (Danshen)
    Irum Naz et al, 2020, Exploration of Targeted Anti-tumor Therapy CrossRef
  10. Dihydroisotanshinone I combined with radiation inhibits the migration ability of prostate cancer cells through DNA damage and CCL2 pathway
    I-Yun Lee et al, 2018, BMC Pharmacology and Toxicology CrossRef
  11. Tanshinone IIA regulates colorectal cancer apoptosis via attenuation of Parkin‑mediated mitophagy by suppressing AMPK/Skp2 pathways
    Lili He et al, 2018, Molecular Medicine Reports CrossRef