The effect of warm rolling temperature on microstructure and texture of microcarbon dual-phase (DP) steel was investigated through scanning electron microscopy (SEM), electron backscatter diffraction (EBSD), and transmission electron microscopy (TEM). The results showed that with the increase of rolling temperature, the density and thickness of the deformation band first increased and then decreased. Ferrite and fine martensite were observed in the annealed sheet, and the ferrite had a much more homogeneous distribution in the sample rolled at 450 °C. During warm rolling, the ferrite developed a dominant γ-fiber and a weak α-texture. During the annealing of the rolled sheet, the intensity of the γ-fiber was increased and a weak {001}<100> texture developed in the sample rolled at room temperature. An increase in the rolling temperature generated an initial decrease and subsequent increase in the strength of the unfavorable {001}<110> texture in the annealed sheet. In addition, the strength reached a maximum at 550 °C due to an increase in the dissolved carbon in the matrix, which was result of carbide dissolution. By contrast, the intensity of the γ-fiber remained relatively higher and was deemed the weaker {001}<110> component in the annealed sheet rolled at 450 °C. Therefore, a larger texture factor (fγ-fiber/f(α-fiber+λ-fiber)) can be produced under this process.

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The pathogenesis mechanism of lung cancer is very complex, with high incidence and mortality. Serpin family A member 3 (SERPINA3) expression levels were reduced in the sera of patients with lung cancer and may be a candidate diagnostic and prognostic survival biomarker in lung cancer, as previously reported. However, the detailed biological functions of SERPINA3 in the pathogenesis of lung cancer remain unknown. In the present study, it was aimed to explore the effects of SERPINA3 on the occurrence of lung cancer. SERPINA3 expression was assessed using bioinformatics database analysis and experimental detection. Then, the biological effects of SERPINA3 were investigated in a cell culture system and a xenograft model of human lung cancer. The potential regulatory mechanism of SERPINA3 in lung cancer was explored by data-independent acquisition mass spectrometry (DIA-MS) detection and further validated by western blotting (WB). The results indicated that SERPINA3 expression levels were significantly downregulated in lung cancer tissues and cell lines. At the cellular level, it was revealed that overexpressed SERPINA3 inhibited cell growth, proliferation, migration and invasion and promoted the apoptosis of lung cancer cells. Moreover, overexpressed SERPINA3 enhanced the sensitivity of lung cancer cells to osimertinib. In vivo , a xenograft model of human lung cancer was established with BALB/c nude mice. After the injection of A549 cells, the tumor growth of the tumor-bearing mice in the SERPINA3-overexpressing group increased more slowly, and the tumor volume was smaller than that in the empty-vector group. Mechanistically, a total of 65 differentially expressed proteins were identified. It was found that the speckle-type POZ protein (SPOP) was significantly upregulated in SERPINA3-overexpressing H157 cells using DIA-MS detection and analysis. WB validation showed that SPOP expression increased, and NF-kappaB (NF-κB) p65 was inhibited in cell lines and tumor tissues of mice when SERPINA3 was overexpressed. The present findings suggest that SERPINA3 is involved in the development of lung cancer and has an antineoplastic role in lung cancer.