Esophageal squamous cell carcinoma (ESCC) is prevalent in some geographical regions of the world. ESCC development presents a multistep pathogenic process from inflammation to invasive cancer; however, what is critical in these processes and how they evolve is largely unknown, obstructing early diagnosis and effective treatment. Here, we create a mouse model mimicking human ESCC development and construct a single-cell ESCC developmental atlas. We identify a set of key transitional signatures associated with oncogenic evolution of epithelial cells and depict the landmark dynamic tumorigenic trajectories. An early downregulation of CD8 + response against the initial tissue damage accompanied by the transition of immune response from type 1 to type 3 results in accumulation and activation of macrophages and neutrophils, which may create a chronic inflammatory environment that promotes carcinogen-transformed epithelial cell survival and proliferation. These findings shed light on how ESCC is initiated and developed.

We report the results of an experimental study of the correlations between line edge roughness (LER) and aerial image contrast for different lithographies in identical processing conditions. The characterization has been performed using atomic force microscopy carbon nanotube tips to image the top and bottom of trenches with very high resolution. Experimental results generally support that higher aerial image contrast leads to lower line edge roughness, but differences exist among the lithographies and resists. Top surface roughness results show similar trends with LER. Higher aerial image modulation also yields higher resist sidewall angle.

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Magnetic recyclable PtyCo1−y/Ti3C2X2 (X = O, F) catalyst exhibits excellent catalytic performance for the hydrolysis of AB at room temperature.

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