Endoplasmic reticulum stress-a key guardian in cancer.
Wenlong ZhangYidan ShiLinda OyangShiwen CuiShizhen LiJinyun LiLin LiuYun LiMingjing PengShiming TanLongzheng XiaJinguan LinXuemeng XuNayiyuan WuQiu PengYanyan TangXia LuoQianjin LiaoXianjie JiangYujuan ZhouPublished in: Cell death discovery (2024)
Endoplasmic reticulum stress (ERS) is a cellular stress response characterized by excessive contraction of the endoplasmic reticulum (ER). It is a pathological hallmark of many diseases, such as diabetes, obesity, and neurodegenerative diseases. In the unique growth characteristic and varied microenvironment of cancer, high levels of stress are necessary to maintain the rapid proliferation and metastasis of tumor cells. This process is closely related to ERS, which enhances the ability of tumor cells to adapt to unfavorable environments and promotes the malignant progression of cancer. In this paper, we review the roles and mechanisms of ERS in tumor cell proliferation, apoptosis, metastasis, angiogenesis, drug resistance, cellular metabolism, and immune response. We found that ERS can modulate tumor progression via the unfolded protein response (UPR) signaling of IRE1, PERK, and ATF6. Targeting the ERS may be a new strategy to attenuate the protective effects of ERS on cancer. This manuscript explores the potential of ERS-targeted therapies, detailing the mechanisms through which ERS influences cancer progression and highlighting experimental and clinical evidence supporting these strategies. Through this review, we aim to deepen our understanding of the role of ER stress in cancer development and provide new insights for cancer therapy.
Keyphrases
- endoplasmic reticulum stress
- papillary thyroid
- induced apoptosis
- squamous cell
- immune response
- endoplasmic reticulum
- cell proliferation
- cancer therapy
- type diabetes
- lymph node metastasis
- cardiovascular disease
- young adults
- stem cells
- oxidative stress
- squamous cell carcinoma
- insulin resistance
- drug delivery
- adipose tissue
- transcription factor
- skeletal muscle
- binding protein
- breast cancer cells
- toll like receptor
- weight gain
- sensitive detection
- estrogen receptor