Chen Ruoxue, Huang Xuan, Hou Jiayun, Ni Junjie, Zhao Wenrui, Li Quanlin, Jiao Heng, Cao Xin
Institute of Clinical Science, Zhongshan Hospital, Fudan University Shanghai Medical College, Shanghai, China.
Endoscopy Center and Endoscopy Research Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Clin Transl Med. 2025 Jan;15(1):e70148. doi: 10.1002/ctm2.70148.
Oesophageal cancer ranks among the most prevalent malignant tumours globally, primarily consisting of oesophageal squamous cell carcinoma (ESCC). Cancer stem cells (CSCs) accelerate the progression ESCC via their strong self-renewal and tumourigenic capabilities, presenting significant clinical challenges due to increased risks of recurrence and drug resistance.
Our previous study has reported WYC-209, which is capable of inducing apoptosis of CSCs in melanoma and hepatoma, but is ineffective against ESCC. Additionally, clinical studies in ESCC still lack drug candidates that effectively target CSCs. Therefore, our team developed a series of novel retinoids that target retinoic acid receptors (RARs), with enhanced potency, broader efficacy and minimised toxic side effects against CSCs. Following iterative optimisation and pharmacological validation, ZSH-2208 was identified as the most promising candidate for effectively targeting ESCC tumour-repopulating cells (TRCs). Mechanistic exploration revealed that ZSH-2208 inhibits the growth of ESCC-TRCs through modulation of the RARγ-TNFAIP3 axis. The clinical significance of the key molecule TNFAIP3 in ESCC has also been demonstrated.
This study introduces ZSH-2208, a novel retinoid specifically targeting ESCC-TRCs, which holds significant potential for clinical application in ESCC.
The ESCC-TRCs replicates the characteristics of ESCC stem cells, which are inhibited by ZSH-2208. In vivo and in vitro experiments demonstrated that ZSH-2208, a novel RA analogue, effectively inhibits the growth of ESCC-TRCs through the RARγ-TNFAIP3 axis. Low levels of TNFIP3 protein may be associated with improved survival probability in ESCC patients.
食管癌是全球最常见的恶性肿瘤之一,主要由食管鳞状细胞癌(ESCC)组成。癌症干细胞(CSCs)通过其强大的自我更新和致瘤能力加速ESCC的进展,由于复发风险和耐药性增加,带来了重大的临床挑战。
我们之前的研究报道了WYC-209,它能够诱导黑色素瘤和肝癌中的CSCs凋亡,但对ESCC无效。此外,ESCC的临床研究仍然缺乏有效靶向CSCs的候选药物。因此,我们的团队开发了一系列新型视黄酸,它们靶向视黄酸受体(RARs),对CSCs具有更强的效力、更广泛的疗效和最小化的毒副作用。经过迭代优化和药理学验证,ZSH-2208被确定为有效靶向ESCC肿瘤再增殖细胞(TRCs)的最有前景的候选药物。机制探索表明,ZSH-2208通过调节RARγ-TNFAIP3轴抑制ESCC-TRCs的生长。关键分子TNFAIP3在ESCC中的临床意义也得到了证实。
本研究介绍了ZSH-2208,一种特异性靶向ESCC-TRCs的新型视黄酸,在ESCC临床应用中具有巨大潜力。
ESCC-TRCs复制了ESCC干细胞的特征,被ZSH-2208抑制。体内和体外实验表明,新型RA类似物ZSH-2208通过RARγ-TNFAIP3轴有效抑制ESCC-TRCs的生长。低水平的TNFIP3蛋白可能与ESCC患者较高的生存概率相关。