血红蛋白亚基θ1通过降低肺腺癌中的活性氧来促进增殖。
Hemoglobin Subunit Theta 1 Promotes Proliferation by Reducing Reactive Oxygen Species in Lung Adenocarcinoma.
作者信息
Kim Kyungho, Choi Eun-Young, Ahn Hye-Mi, Kim Dong-Gun, Kim Youn-Jae
机构信息
Targeted Therapy Branch, Division of Rare and Refractory Cancer, Research Institute, National Cancer Center, Goyang 10408, Republic of Korea.
出版信息
Cancers (Basel). 2023 Nov 21;15(23):5504. doi: 10.3390/cancers15235504.
Lung adenocarcinoma is a crucial contributor to cancer-related mortality; however, effective treatments remain challenging. The present study aimed to investigate the role of hemoglobin subunit theta 1 (HBQ1), an α subunit of hemoglobin whose expression has recently been reported in non-erythroid cells, in lung adenocarcinoma. Comparative analysis showed that HBQ1 expression was significantly higher in lung adenocarcinoma tissues compared to normal lung tissues. Moreover, high HBQ1 expression was correlated with unfavorable overall survival and progression-free survival in patients, highlighting its potential as a prognostic marker. Our functional experiments revealed that when overexpressed, HBQ1 acts as an oncogene, enhancing cell proliferation, whereas HBQ1 knockdown inhibits it. Additionally, HBQ1 exhibited antioxidant properties by reducing basal reactive oxygen species levels, playing a crucial role in lung adenocarcinoma progression. These findings emphasize the critical role of HBQ1 in driving tumor growth and progression in lung adenocarcinoma. Our in vivo studies further supported the role of HBQ1 in lung adenocarcinoma. HBQ1 knockdown resulted in the inhibition of lung adenocarcinoma growth, demonstrating the potential of HBQ1 as a therapeutic target. Our findings highlight the importance of HBQ1 in lung adenocarcinoma and suggest its potential as both a diagnostic marker and a molecular target for therapeutic interventions.
肺腺癌是导致癌症相关死亡的一个关键因素;然而,有效的治疗方法仍然具有挑战性。本研究旨在探讨血红蛋白亚基θ1(HBQ1)在肺腺癌中的作用,HBQ1是血红蛋白的一个α亚基,最近有报道称其在非红细胞中表达。比较分析表明,与正常肺组织相比,肺腺癌组织中HBQ1的表达显著更高。此外,高HBQ1表达与患者不良的总生存期和无进展生存期相关,突出了其作为预后标志物的潜力。我们的功能实验表明,过表达时,HBQ1作为一种癌基因发挥作用,增强细胞增殖,而敲低HBQ1则抑制细胞增殖。此外,HBQ1通过降低基础活性氧水平表现出抗氧化特性,在肺腺癌进展中起关键作用。这些发现强调了HBQ1在推动肺腺癌肿瘤生长和进展中的关键作用。我们的体内研究进一步支持了HBQ1在肺腺癌中的作用。敲低HBQ1导致肺腺癌生长受到抑制,证明了HBQ1作为治疗靶点的潜力。我们的发现突出了HBQ1在肺腺癌中的重要性,并表明其作为诊断标志物和治疗干预分子靶点的潜力。