Long noncoding RNA CASC2 alleviates the growth, migration and invasion of oral squamous cell carcinoma via downregulating CDK1.

Since this article has been suspected of research misconduct and the corresponding authors did not respond to our request to prove originality of data and figures, "Long noncoding RNA CASC2 alleviates the growth, migration and invasion of oral squamous cell carcinoma via downregulating CDK1, by H.-B. Xing, H.-M. Qiu, Y. Li, P.-F. Dong, X.-M. Zhu, published in Eur Rev Med Pharmacol Sci 2019; 23 (11): 4777-4783-DOI: 10.26355/eurrev_201906 _18060-PMID: 31210307" has been withdrawn. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/18060.

[Surgical concept and techniques of recurrent cervical cancer patients accompanied with high risk of intestinal obstruction after radical radiotherapy].

Objective: To explore the method of relieving intestinal obstruction in patients with recurrent cervical cancer accompanied with intestinal obstruction after radical radiotherapy. Methods: The data of 10 recurrent cervical cancer patients accompanied with high risk weak constitution and intestinal obstruction after radical radiotherapy from May 2012 to May 2018 were retrospectively analyzed, including preoperative radiotherapy dose, physique and obstruction status, operation time, operation blood loss, postoperative digestive tract patency and diet. All of the 10 patients with cervical cancer recurrence accompanied with intestinal obstruction and disturbance of independent walking after radical radiotherapy. Results: The median fasting time of the 10 patients was 21 days, the median weight was 35.5 kg, the median body mass index (BMI) was 13.3 kg/m(2,) the median value of hemoglobin was 67 g/L, and the median value of platelet was 44×10(9) /L. All of the patients underwent enterostomy. the median operation time was 6.0 min and the median amount of bleeding was 5.0 ml. All of the patients defecated after operation, fed on the first day after operation, and were able to walk on their own 5 days after operation. Conclusions: Although the cervical cancer patients with recurrent intestinal obstruction after radical radiotherapy are extremely weak, some patients still have the opportunity to relieve intestinal obstruction if the treatment strategy and surgical method are appropriate.

Long noncoding RNA CASC2 alleviates the growth, migration and invasion of oral squamous cell carcinoma via downregulating CDK1.

OBJECTIVE: Recent studies have revealed the important role of long noncoding RNAs (lncRNAs) in regulating the progression of tumorigenesis. Oral squamous cell carcinoma (OSCC) is a prevalent tumor in the world. This study aims to identify the specific mechanism of lncRNA CASC2 in alleviating the progression of OSCC. PATIENTS AND METHODS: CASC2 expression in OSCC cell lines and 40 paired OSCC samples were detected by quantitative Real-time polymerase chain reaction (qRT-PCR). Moreover, in vitro functions of CASC2 in regulating the cellular behaviors of OSCC cells were identified by performing transwell assay, wound healing assay and proliferation assay. The underlying mechanism of CASC2 in mediating the progression of OSCC was explored by qRT-PCR and Western blot. RESULTS: CASC2 expression was remarkably downregulated in OSCC tissues compared with that in adjacent normal samples. Moreover, proliferation, invasion and migration were inhibited in OSCC cells overexpressing CASC2. CASC2 overexpression in OSCC cells downregulated CDK1 at both mRNA and protein levels in vitro. Besides, the expression of CDK1 in OSCC tissues was negatively correlated to the expression of CASC2. CONCLUSIONS: CASC2 suppresses the migration, invasion and proliferation of OSCC cells through downregulating CDK1, which may offer a new therapeutic intervention for OSCC patients.

Direct quantification of mono- and di-D-α-tocopherol polyethylene glycol 1000 succinate by high performance liquid chromatography.

A simple and direct reversed-phase high performance liquid chromatography (RP-HPLC) method with UV detection was developed and validated for the determination of mono- and di-D-α-tocopherol polyethylene glycol 1000 succinate (TPGS 1000) in TPGS mixture. Before the HPLC analysis, mono- and di-TPGS 1000 were separated by simulated moving bed (SMB) chromatography system and characterized by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The mass spectrometric results confirmed that the molar mass distribution of TPGS prepared in our laboratory was very close to that of the product of Eastman Chemical Company with similar n¯ (average polymerization degree), M(n)¯ (number-average molecular weight) and M(w)¯ (weight-average molecular weight). The HPLC analysis was carried out on a C30 analytical column with mobile phases comprised of acetonitrile (A) and isopropanol (B) in gradient conditions. Validation of the analytical method was done on the following parameters: system suitability, linearity, limits of detection and quantification, accuracy and precision, method robustness and solution stability. The linearity of the calibration curves for mono- and di-TPGS 1000 from both sources was found to be good (r(2)>0.9996). The recovery values were from 94.6% to 103.3% for mono-TPGS, and 93.5% to 103.3% for di-TPGS. This method could be successfully used in the direct quantification of mono- and di-TPGS in TPGS 1000 mixture using TPGS standards with similar molecular mass distributions although derived from different sources.