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TMED3的表达与结直肠癌预后独立相关。

Expression of TMED3 is independently associated with colorectal cancer prognosis.

作者信息

Wang Rong-Fei, Hong Yong-Gang, Hao Li-Qiang, Yu Hai-Tao

机构信息

Department of Tumor, Anus and Intestine, Jinhua People's Hospital, Jinhua, Zhejiang 321000, P.R. China.

Department of Colorectal Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, P.R. China.

出版信息

Exp Ther Med. 2022 Apr;23(4):286. doi: 10.3892/etm.2022.11215. Epub 2022 Feb 15.

DOI:10.3892/etm.2022.11215
PMID:35317448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8908477/
Abstract

Colorectal cancer (CRC) is the third most common cancer type and one of the deadliest cancers worldwide. Transmembrane p24 trafficking protein 3 (TMED3) has previously been indicated to suppress CRC metastasis, but its clinical significance has remained undetermined. In the present study, the expression of TMED3 was indicated to be elevated at the mRNA and protein levels in CRC tumor samples relative to that in para-cancerous healthy tissue samples (P<0.05). Furthermore, Kaplan-Meier survival analysis revealed a significant negative association between elevated TMED3 protein levels and overall survival of patients with CRC (P<0.001, log-rank test). Multivariate Cox regression analysis additionally determined that elevated TMED3 expression in primary CRC tumors was an independent predictor of poor prognosis (P<0.05). These results revealed that elevated TMED3 expression in CRC was associated with patient survival outcomes, suggesting that TMED3 may be a potential prognostic biomarker for this cancer type.

摘要

结直肠癌(CRC)是全球第三大常见癌症类型,也是最致命的癌症之一。跨膜p24转运蛋白3(TMED3)此前已被证明可抑制结直肠癌转移,但其临床意义仍未明确。在本研究中,相对于癌旁健康组织样本,结直肠癌肿瘤样本中TMED3在mRNA和蛋白质水平的表达均升高(P<0.05)。此外,Kaplan-Meier生存分析显示,TMED3蛋白水平升高与结直肠癌患者的总生存期之间存在显著负相关(P<0.001,对数秩检验)。多变量Cox回归分析还确定,原发性结直肠癌肿瘤中TMED3表达升高是预后不良的独立预测因素(P<0.05)。这些结果表明,结直肠癌中TMED3表达升高与患者生存结果相关,提示TMED3可能是这种癌症类型的潜在预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/809186b04b3a/etm-23-04-11215-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/640654827e59/etm-23-04-11215-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/5ba890982114/etm-23-04-11215-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/809186b04b3a/etm-23-04-11215-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/640654827e59/etm-23-04-11215-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/5ba890982114/etm-23-04-11215-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd0/8908477/809186b04b3a/etm-23-04-11215-g02.jpg

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本文引用的文献

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The protein secretion modulator TMED9 drives CNIH4/TGFα/GLI signaling opposing TMED3-WNT-TCF to promote colon cancer metastases.蛋白分泌调节剂 TMED9 驱动 CNIH4/TGFα/GLI 信号转导,与 TMED3-WNT-TCF 相反,促进结肠癌转移。
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TMED2/emp24 is required in both the chorion and the allantois for placental labyrinth layer development.胎盘迷路层发育过程中,绒毛膜和尿囊都需要TMED2/emp24。
Dev Biol. 2018 Dec 1;444(1):20-32. doi: 10.1016/j.ydbio.2018.09.012. Epub 2018 Sep 17.
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Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
两种含环己基甘氨酸配体的抗癌铂配合物对结肠癌细胞系的生物活性:理论与实验研究
ACS Omega. 2022 Oct 5;7(44):39794-39811. doi: 10.1021/acsomega.2c03776. eCollection 2022 Nov 8.
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J Cancer Res Clin Oncol. 2023 Jul;149(7):3485-3494. doi: 10.1007/s00432-022-04257-x. Epub 2022 Aug 11.
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Dysregulation of Circadian Clock Genes Associated with Tumor Immunity and Prognosis in Patients with Colon Cancer.生物钟基因失调与结肠癌患者的肿瘤免疫和预后相关。
Comput Math Methods Med. 2022 Jul 16;2022:4957996. doi: 10.1155/2022/4957996. eCollection 2022.
全球癌症统计数据 2018:GLOBOCAN 对全球 185 个国家/地区 36 种癌症的发病率和死亡率的估计。
CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
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TMED3 promotes hepatocellular carcinoma progression via IL-11/STAT3 signaling.TMED3 通过 IL-11/STAT3 信号促进肝癌进展。
Sci Rep. 2016 Nov 30;6:37070. doi: 10.1038/srep37070.
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Colorectal Cancer on the Decline--Why Screening Can't Explain It All.结直肠癌发病率呈下降趋势——为何筛查无法完全解释这一现象。
N Engl J Med. 2016 Apr 28;374(17):1605-7. doi: 10.1056/NEJMp1600448.
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The COP II adaptor protein TMED7 is required to initiate and mediate the delivery of TLR4 to the plasma membrane.COP II衔接蛋白TMED7是启动和介导Toll样受体4(TLR4)转运至质膜所必需的。
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