Mechanisms of cancer cell death induction by triptolide.
Ali Hamid AbdulHusseinMuataz Mohammed Al-TaeeZahra Abdul RadihDhuha Salman AljubooryZainab Qasim MohammedTabarak Sami HasheshYassine RiadiSalema K HadrawiMasoud NajafiPublished in: BioFactors (Oxford, England) (2023)
Drug resistance is a hot topic issue in cancer research and therapy. Although cancer therapy including radiotherapy and anti-cancer drugs can kill malignant cells within the tumor, cancer cells can develop a wide range of mechanisms to resist the toxic effects of anti-cancer agents. Cancer cells may provide some mechanisms to resist oxidative stress and escape from apoptosis and attack by the immune system. Furthermore, cancer cells may resist senescence, pyroptosis, ferroptosis, necroptosis, and autophagic cell death by modulating several critical genes. The development of these mechanisms leads to resistance to anti-cancer drugs and also radiotherapy. Resistance to therapy can increase mortality and reduce survival following cancer therapy. Thus, overcoming mechanisms of resistance to cell death in malignant cells can facilitate tumor elimination and increase the efficiency of anti-cancer therapy. Natural-derived molecules are intriguing agents that may be suggested to be used as an adjuvant in combination with other anticancer drugs or radiotherapy to sensitize cancer cells to therapy with at least side effects. This paper aims to review the potential of triptolide for inducing various types of cell death in cancer cells. We review the induction or resistance to different cell death mechanisms such as apoptosis, autophagic cell death, senescence, pyroptosis, ferroptosis, and necrosis following the administration of triptolide. We also review the safety and future perspectives for triptolide and its derivatives in experimental and human studies. The anticancer potential of triptolide and its derivatives may make them effective adjuvants for enhancing tumor suppression in combination with anticancer therapy.
Keyphrases
- cell death
- cell cycle arrest
- cancer therapy
- early stage
- oxidative stress
- drug delivery
- induced apoptosis
- endothelial cells
- radiation therapy
- papillary thyroid
- locally advanced
- radiation induced
- squamous cell carcinoma
- gene expression
- stem cells
- cell proliferation
- cardiovascular disease
- squamous cell
- nlrp inflammasome
- risk assessment
- dna methylation
- pi k akt
- stress induced
- lymph node metastasis
- smoking cessation
- heat stress
- drug induced
- cell therapy
- replacement therapy
- pluripotent stem cells