The reducing effect of TNF-α on carbonic anhydrase III gene expression in colon carcinoma and osteosarcoma cells.

IF 2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Cytotechnology Pub Date : 2025-08-01 Epub Date: 2025-07-15 DOI:10.1007/s10616-025-00815-6
Sümeyye Aydoğan Türkoğlu, Derya Okuyan, Feray Köçkar
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引用次数: 0

Abstract

The appropriate acid-base balance in organisms is maintained by Carbonic Anhydrase proteins (CAs), which have hydratase activity and regulate intracellular pH. CAs are required for both physiological and pathophysiological processes such as cancer development, and there are differences in their expression profiles in different cancer types. Some members of the CA family like CAIX and CAXII have been suggested as potential cancer biomarkers in various studies. CAIX has been proposed as a possible biomarker for hypoxic colorectal carcinoma. Expression of CAIII, another member of the CA family, was also found to be reduced by TGF-β via the MAPK and PI3K signaling pathways in human colon cancer cells. Additionally, not much is known regarding the interaction between TNF-α, inflammation-related cytokine, and CAIII in colorectal carcinoma (CRC). This study investigates the effect of TNF-α on CAIII expression in different cancer cells, namely HT-29 and Saos-2. CAIII mRNA expression was analyzed by qRT-PCR at both late (24, 48, and 72 h) and early time points (1, 3, and 6 h). Western blot analysis was also used to confirm the reducing effect of TNF-α at the CAIII protein level. To analyze the transcriptional regulation of CAIII by TNF-α, CAIII promoter constructs were transiently transfected to HT-29 and Saos-2 cells, and transcriptional activities of truncated promoter constructs were analyzed with luciferase/SEAP activities. 500U/mL TNF-α led to a drastic decrease at 24 and 48 h time points at CAIII mRNA level. Western blot analysis showed that this decreasing effect of 500 U/mL TNF-α at 24 h, 48 h, and 72 h resulted in a reduction of the CAIII protein level by 0.5 times. P1 (- 939/+ 86), P2 (- 699/+ 86), P3 (- 236/+ 86), and P4 (- 108/+ 86) CAIII promoter constructs were transiently transfected to HT-29 cells, P4 (- 108/+ 86) promoter basal activity is greater than the other promoter constructs. Transcriptional activity of all CAIII promoter constructs was reduced by TNF-α. As a result of pathway inhibition analysis, we deduce that TNF- α decreases CAIII mRNA expression in a colon cancer cell via the PI3K pathway. In addition, the similar reducing effect of TNF-α on CAIII in Saos-2 cells, which is a model of osteosarcoma, was also obtained at mRNA and transcriptional levels.

Supplementary information: The online version contains supplementary material available at 10.1007/s10616-025-00815-6.

TNF-α对结肠癌和骨肉瘤细胞碳酸酐酶III基因表达的降低作用。
生物体内适当的酸碱平衡是由碳酸酐酶蛋白(CAs)维持的,它具有水合酶活性并调节细胞内ph。CAs在癌症发生等生理和病理生理过程中都是必需的,在不同类型的癌症中它们的表达谱存在差异。CA家族的一些成员,如CAIX和CAXII,已在各种研究中被认为是潜在的癌症生物标志物。CAIX被认为可能是低氧结直肠癌的生物标志物。CA家族的另一成员CAIII的表达也被发现通过MAPK和PI3K信号通路被TGF-β降低。此外,对于结直肠癌(CRC)中TNF-α、炎症相关细胞因子和CAIII之间的相互作用知之甚少。本研究探讨TNF-α对不同肿瘤细胞HT-29和Saos-2中CAIII表达的影响。在晚(24、48和72 h)和早(1、3和6 h)时间点采用qRT-PCR分析CAIII mRNA的表达。Western blot分析证实TNF-α在CAIII蛋白水平的降低作用。为了分析TNF-α对CAIII的转录调控作用,我们将CAIII启动子构建物瞬时转染HT-29和Saos-2细胞,并用荧光素酶/SEAP活性分析截断的启动子构建物的转录活性。500U/mL TNF-α可在24和48 h时显著降低CAIII mRNA水平。Western blot分析显示,500 U/mL TNF-α在24 h、48 h和72 h的降低作用导致CAIII蛋白水平降低0.5倍。将P1(- 939/+ 86)、P2(- 699/+ 86)、P3(- 236/+ 86)和P4 (- 108/+ 86) CAIII启动子瞬时转染HT-29细胞,P4(- 108/+ 86)启动子的基础活性高于其他启动子。TNF-α降低了所有CAIII启动子的转录活性。作为途径抑制分析的结果,我们推断TNF- α通过PI3K途径降低结肠癌细胞中CAIII mRNA的表达。此外,在骨肉瘤模型Saos-2细胞中,TNF-α在mRNA和转录水平上也获得了类似的降低CAIII的作用。补充信息:在线版本包含补充资料,可在10.1007/s10616-025-00815-6获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cytotechnology
Cytotechnology 生物-生物工程与应用微生物
CiteScore
4.10
自引率
0.00%
发文量
49
审稿时长
6-12 weeks
期刊介绍: The scope of the Journal includes: 1. The derivation, genetic modification and characterization of cell lines, genetic and phenotypic regulation, control of cellular metabolism, cell physiology and biochemistry related to cell function, performance and expression of cell products. 2. Cell culture techniques, substrates, environmental requirements and optimization, cloning, hybridization and molecular biology, including genomic and proteomic tools. 3. Cell culture systems, processes, reactors, scale-up, and industrial production. Descriptions of the design or construction of equipment, media or quality control procedures, that are ancillary to cellular research. 4. The application of animal/human cells in research in the field of stem cell research including maintenance of stemness, differentiation, genetics, and senescence, cancer research, research in immunology, as well as applications in tissue engineering and gene therapy. 5. The use of cell cultures as a substrate for bioassays, biomedical applications and in particular as a replacement for animal models.
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