Gene expression changes in human lung cells exposed to arsenic, chromium, nickel or vanadium indicate the first steps in cancer
文献信息
Hailey A. Clancy, Hong Sun, Lisa Passantino, Thomas Kluz, Alexandra Muñoz, Jiri Zavadil, Max Costa
The complex process of carcinogenesis begins with transformation of a single cell to favor aberrant traits such as loss of contact inhibition and unregulated proliferation – features found in every cancer. Despite cancer's widespread prevalence, the early events that initiate cancer remain elusive, and without knowledge of these events cancer prevention is difficult. Here we show that exposure to As, Cr, Ni, or vanadium (V) promotes changes in gene expression that occur in conjunction with aberrant growth. We exposed immortalized human bronchial epithelial cells to one of four metals/metalloid for four to eight weeks and selected transformed clonal populations based upon anchorage independent growth of single cells in soft agar. We detected a metal-specific footprint of cancer-related gene expression that was consistent across multiple transformed clones. These gene expression changes persisted in the absence of the progenitor metal for numerous cell divisions. Our results show that even a brief exposure to a carcinogenic metal may cause many changes in gene expression in the exposed cells, and that from these many changes, the specific change(s) that each metal causes that initiate cancer likely arise.
相关文献
IF 6.367
Carbon-based photocatalysts for enhanced photocatalytic reduction of CO2 to solar fuelsIF 6.367
Near infrared light activation of an injectable whole-cell cancer vaccine for cancer immunoprophylaxis and immunotherapyIF 6.843
Performance of electrode-supported silica membrane separators in lithium-ion batteriesIF 6.367
Transition-metal-free insertion reactions of alkynes into the C–N σ-bonds of imides: synthesis of substituted enamides or chromonesIF 6.222
Stabilizing synthetic DNA for long-term data storage with earth alkaline saltsIF 6.222
Synthesis and hydrogen evolving catalysis of a panchromatic photochemical molecular deviceIF 6.367
Chemoproteomics-based target profiling of sinomenine reveals multiple protein regulators of inflammationIF 6.222
Synthesis of aviation fuel from bio-derived isophoroneIF 6.367
Co-production of pure hydrogen, carbon dioxide and nitrogen in a 10 kW fixed-bed chemical looping systemIF 6.367
来源期刊
Metallomics

Metallomics publishes cutting-edge investigations aimed at elucidating the identification, distribution, dynamics, role and impact of metals and metalloids in biological systems. Studies that address the “what, where, when, how and why” of these inorganic elements in cells, tissues, organisms, and various environmental niches are welcome, especially those employing multidisciplinary approaches drawn from the analytical, bioinorganic, medicinal, environmental, biophysical, cell biology, plant biology and chemical biology communities. We are particularly interested in articles that enhance our chemical and/or physical understanding of the molecular mechanisms of metal-dependent life processes, and those that probe the common space between metallomics and other ‘omics approaches to uncover new insights into biological processes. Metallomics seeks to position itself at the forefront of those advances in analytical chemistry destined to clarify the enormous complexity of biological systems. As such, we particularly welcome those papers that outline cutting-edge analytical technologies, e.g., in the development and application of powerful new imaging, spectroscopic and mass spectrometric modalities. Work that describes new insights into metal speciation, trafficking and dynamics in complex systems or as a function of microenvironment are also strongly encouraged. Studies that examine the interconnectivity of metal-dependent processes with systems level responses relevant to organismal health or disease are also strongly encouraged, for example those that probe the effect of chemical exposure on metal homeostasis or the impact of metal-based drugs on cellular processes.