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Gang Wang Jun-Jie Wang Pei-Hao Yin Ke Xu Yu-Zhu Wang Feng Shi Jing Gao Xing-Li Fu 《Journal of cellular biochemistry》2019,120(2):1106-1121
Alterations in cellular energy metabolism play critical roles in colorectal cancer (CRC). These alterations, which correlate to KRAS mutations, have been identified as energy metabolism signatures. This review summarizes the relationship between colorectal tumors associated with mutated KRAS and energy metabolism, especially for the deregulated energy metabolism that affects tumor cell proliferation, invasion, and migration. Furthermore, this review will concentrate on the role of metabolic genes, factors and signaling pathways, which are coupled with the primary energy source connected with the KRAS mutation that induces metabolic alterations. Strategies for targeting energy metabolism in mutated KRAS CRC are also introduced. In conclusion, deregulated energy metabolism has a close relationship with KRAS mutations in colorectal tumors. Therefore, selective inhibitors, agents against metabolic targets or KRAS signaling, may be clinically useful for colorectal tumor treatment through a patient-personalized approach. 相似文献
994.
YouZu Xu Jian Lin YingYing Jin Meifang Chen HaiHong Zheng JiaXi Feng 《Journal of cellular biochemistry》2019,120(10):17413-17421
Aberrant expression of long noncoding RNAs (lncRNAs) contributes to all phenotypes of cancer including metastasis, which is a major cause of death in many advanced malignancies. One particular lncRNA, H19, is found to be a crucial player in cancer progression by modulating multiple microRNAs (miRNAs). In this study, we screened miRNAs possibly associated with H19 using lung carcinoma cell lines and patient with lung cancer tissues, and selected one possible hit, hsa-miR-6515-3p, to perform in vitro functional assays. Its inhibition leads to decreased proliferation and migration of SPC-A1 lung cancer cells and is in good correlation with H19-knockdown groups. These results indicate that H19 may be an epigenetic regulator of miR-6515-3p, and its dysregulation may contribute to lung cancer progression and metastasis. 相似文献
995.
Yiying Zeng Gadi V. P. Reddy Zhihong Li Yujia Qin Yannan Wang Xubin Pan Fan Jiang Feng Gao Zi‐Hua Zhao 《Journal of Applied Entomology》2019,143(3):165-176
Since the start of the 20th century, many invasive alien species (IAS) have spread rapidly around the world, causing serious threats to economies, societies and the environment. Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) is an important quarantine insect species in many countries that spread around the world over the last century. This review collected information on the distribution of B. dorsalis to explore the patterns of its invasion expansion. We found B. dorsalis to be distributed in 75 countries (comprised of 124 geographical distribution regions: provinces or states) in Asia, Africa, North America, South America and Oceania up to 2017. Asia and Africa were the most represented regions, accounting for 86.3% of the total number of countries. From 1910 to 1990, B. dorsalis was only found in five countries, but in the last three decades, it has experienced a sharp increase in its rate of spread, invading 70 more countries. Global temperature anomaly has significantly positive correlation with the spread of B. dorsalis. The results of this review provide a theoretical basis for understanding and predicting the continued spread of B. dorsalis under global changes. 相似文献
996.
同翅类昆虫的雄性生殖系统及精子发生(昆虫纲:半翅目) 总被引:3,自引:1,他引:2
本文比较了同翅类昆虫雄性生殖系统的结构、减数分裂期间染色体的行为和精子尾部的超微结构。研究表明蜡蝉总科和异翅类的精巢具有被膜,而蝉总科、叶蝉总科、沫蝉总科、角蝉总科、木虱总科、蚜总科、粉虱总科和蚧总科的精巢均不具有被膜。也可以根据精巢小叶的形状将精巢分为三类,蝉总科、叶蝉总科、沫蝉总科、角蝉总科、蚜总科和粉虱总科的精巢小叶为球形,蜡蝉总科、木虱总科和蚧总科的精巢小叶为管状,而异翅类的精巢小叶为片层状。减数分裂可以被分为5类:①蝉型(Cicadoidtype);②蜡蝉型(Fulgoroidtype);③木虱型(Psyloidtype);④蚜型(Aphidoidtype);⑤粉虱型(Aleyrodoidtype)和⑥蚧型(Coccoidtype),至少具有四个类群的减数分裂前期I具有弥散期,它们是:木虱总科、蜡蝉总科、蚧总科和异翅类。除粉虱总科和蚧总科的精子尾部退化以外,其余种类的精子鞭毛均具有典型的9 9 2轴丝结构。 相似文献
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998.
Feng Guo Chengchun Tang Bo Huang Lifei Gu Jun Zhou Zongyang Mo Chang Liu Yuqing Liu 《Molecules and cells》2022,45(3):122
The aim of this study was to investigating whether lncRNA H19 promotes myocardial fibrosis by suppressing the miR-29a-3p/miR-29b-3p-VEGFA/TGF-β axis. Patients with atrial fibrillation (AF) and healthy volunteers were included in the study, and their biochemical parameters were collected. In addition, pcDNA3.1-H19, si-H19, and miR-29a/b-3p mimic/inhibitor were transfected into cardiac fibroblasts (CFs), and proliferation of CFs was detected by MTT assay. Expression of H19 and miR-29a/b-3p were detected using real-time quantitative polymerase chain reaction, and expression of α-smooth muscle actin (α-SMA), collagen I, collagen II, matrix metalloproteinase-2 (MMP-2), and elastin were measured by western blot analysis. The dual luciferase reporter gene assay was carried out to detect the sponging relationship between H19 and miR-29a/b-3p in CFs. Compared with healthy volunteers, the level of plasma H19 was significantly elevated in patients with AF, while miR-29a-3p and miR-29b-3p were markedly depressed (P < 0.05). Serum expression of lncRNA H19 was negatively correlated with the expression of miR-29a-3p and miR-29b-3p among patients with AF (rs = –0.337, rs = –0.236). Moreover, up-regulation of H19 expression and down-regulation of miR-29a/b-3p expression facilitated proliferation and synthesis of extracellular matrix (ECM)-related proteins. SB431542 and si-VEGFA are able to reverse the promotion of miR-29a/b-3p on proliferation of CFs and ECM-related protein synthesis. The findings of the present study suggest that H19 promoted CF proliferation and collagen synthesis by suppressing the miR-29a-3p/miR-29b-3p-VEGFA/TGF-β axis, and provide support for a potential new direction for the treatment of AF. 相似文献
999.
Overexpression of Skp2 plays a critical role in tumorigenesis and correlates with poor prognosis in human malignancies. Thus, Skp2 has been proposed as an attractive target for anti-tumor interventions. The expression of Skp2 in human colorectal cancer (CRC) and the role of Skp2 in tumorigenic properties and irradiation sensitivities of CRC cells were examined by anchorage-dependent and -independent growth assays, immunoblot, flow cytometry, immunohistochemical staining, ubiquitination analysis, co-immunoprecipitation assay, CRISPR-Cas9-based gene knockout, and xenograft experiments. Skp2 is highly expressed in CRC patient tissues. Blocking Skp2 expression reduces the tumorigenic properties of CRC cells in vitro and in vivo. Depletion of Skp2 confers sensitivity to irradiation of CRC cells. Skp2 deficiency enhances irradiation-induced intrinsic apoptosis by facilitating E3 ligase FBW7-mediated Mcl-1 ubiquitination and degradation. Knockout of Skp2 sensitizes CRC cells to irradiation treatments in vivo. Our findings indicate that Skp2 stabilizes Mcl-1, and targeting Skp2 in combination with traditional radiotherapy might be efficacious in treating CRC.Subject terms: Biological sciences, Ubiquitylation 相似文献