Purpose To explore the relationship between expression of PCNA and COX-2 in the early laryngeal cancer with negative surgical margins and the local recurrence of tumor. Methods Totally 63 patients with early laryngeal cancer were enrolled in this stud-y, CO2 laser surgery was adopted as treatment, the expression of PCNA and COX-2 was detected in the resected tumor tissue and surgi-cal margins, and the survival and tumor recurrence were also observed. Results The positive rate of the expression of PCNA and COX-2 in the 63 patients with early laryngeal cancer tumor tissues were 73. 02% and 71. 43%, while that in the cutting edge were 33. 33% and 30. 16%, respectively. The expression of PCNA and COX-2 in tumor tissue and cutting edge were of all positive in 41 cases and 13 cases, and the positive rate was 65. 08% and 20. 63%, respectively. In the all followed-up patients, 17 cases were detected of local recurrence, the recurrence rate was 26. 98%, and the recurrence rate in the patients with PCNA positive was 71. 43%, while in the patients with COX-2 positive was 73. 68% (P<0. 05). The combined detection of PCNA and COX-2 positive recurrence rate was significantly higher than that of single positive (P<0. 05). Conclusion PCNA and COX-2 in the early laryngeal cancer with negative surgical margins are important biological markers for the evaluation of prognosis of laryngeal cancer patients, and to formulate the subse-quent treatment regimen. The combined detection of two proteins is more reliable for postoperative management.

【Objective】 To explore the effects of long non-coding RNA (lncRNA) small nucleolar molecule RNA host gene 12 (SNHG12) targeting inhibition of miR-495-3p/ phospholipinositol-3-kinase (PI3K)/protein kinase B (Akt) signaling pathway on the proliferation, migration and invasion of prostate cancer cells. 【Methods】 The expressions of SNHG12 and miR-495-3p in prostate cancer tissues and cells (LNCaP, C4-2, DU145) were detected with real-time fluorescence quantitative PCR (qRT-PCR).After DU145 cells were divided into si-NC, si-SNHG12, si-SNHG12+anti-miR-NC and si-SNHG12+anti-miR-495-3p groups, the expressions of SNHG12 and miR-495-3p were detected with qRT-PCR; the targeting relationship between SNHG12 and miR-495-3p was determined with dual luciferase assay; cell proliferation was assessed with MTT assay; cell migration and invasion were evaluated with Transwell assay; the protein expressions of proliferating cell nuclear antigen (PCNA), N-cadherin, and E-cadherin were detected with Western blot. 【Results】 The expressions of SNHG12 were significantly increased, while the expression of miR-495-3P was significantly decreased in prostate cancer tissues and cells (LNCaP, C4-2, DU145) (P<0.05).Knockdown of SNHG12 decreased DU145 cell activity, lowered the protein expressions of PCNA and N-cadherin, reduced the number of migrating and invading cells, but increased the protein expression of E-cadherin (P<0.05).SNHG12 targeted and negatively regulated miR-495-3p, and down-regulation of miR-495-3p reversed the effects of SNHG12 knockdown on the proliferation, migration and invasion of prostate cancer cells.Compared with the si-NC group, the si-SNHG12 group had significantly decreased expressions of p-PI3K and p-Akt (P<0.05).Compared with the si-SNHG12+anti-miR-NC group, the si-SNHG12+anti-miR-495-3p group had significantly increased protein expressions of p-PI3K and p-Akt (P<0.05). 【Conclusion】 lncRNA SNHG12 can promote the proliferation, migration and invasion of prostate cancer cells through targeted inhibition of miR-495-3p/PI3K/Akt signaling pathway.

The purpose of this experiment is to observe the effects of Tongbi capsule on joint lesions in rabbit with rheumatoid arthritis induced by ovalbumin and explore the mechanism in order to provide reference for clinical application of Tongbi capsule. Rheumatoid arthritis in rabbits was induced by subcutaneous injection of emulsions of ovalbumin and Freund's complete adjuvant and intra articular injection of ovalbumin. After successful modeling, 30 New Zealand rabbits with arthritis were randomly divided into model control group, the high, medium and low dose groups of Tongbi capsule (90, 45, 22.5 mg·kg⁻¹) and prednisone group (5 mg·kg⁻¹). Another six normal rabbits were used as normal control group. After 24 hours of modeling, the rabbits in Tongbi capsule groups received intragastric (i.g.) administrations of Tongbi capsule at 90, 45, 22.5 mg·kg⁻¹·d⁻¹, and the rabbits of prednisone group received i.g. administrations of prednisone at 5 mg·kg⁻¹·d⁻¹ for 2 weeks. The rabbits in normal and model groups received the same volume of distilled water at the same time. The swelling degree of rabbit knee joint and local skin temperature were observed daily. After two weeks of administration, pathological changes of rabbit knee joint were examined by magnetic resonance imaging (MRI); the morphological changes of articular cartilage and synovial membrane were observed by microscope; and the contents of interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-α) in serum were detected by enzyme linked immunosorbent assay (ELISA).The results showed that 24 h after modeling, the knee joints of the rabbits were swollen, with red or dark redlocal skin, and fever, elevated local skin temperature and increased diameters of knee joints. Two weeks after modeling, the swelling of rabbit knee joints was obvious in model group; the joint cavities were filled with purulent fluid; joint synovial membranes were obviously thickened, and even joint cavities were fibrotic and cartilage surfaces showed slight defect; the surface of articular cartilage was obvious fibrosis; synovial epithelial cell proliferation was obvious and accompanied by extensive inflammatory cell infiltration; the levels of IL-1 and TNF-α were significantly higher as compared with those seen in model rabbits (<0.05, <0.01). After 1 and 2 weeks of administration, knee joint diameters and local skin temperatures were smaller or lower than thosein model group (<0.05, <0.01); The lesions of joint cartilage and synovial of all rabbits in each group were less than those in model group; IL-1 and TNF-α levels in serum were also lower than those in model group (<0.05, <0.01). The results reveal that high and medium doses of Tongbi capsule can suppress rheumatoid arthritis induced by ovalbumin in rabbits, reduce joint swelling, inhibit synovial epithelial and fiber hyperplasia and inflammatory cell infiltration, and alleviate articular cartilage damage. The mechanism may be associated with decreasing IL-1 and TNF-α levels in serum.