Urinary malate dehydrogenase 2 is a new biomarker for early detection of non-small-cell lung cancer.
Yu-Chen MaPeng-Fei TianZhi-Peng ChenDong-Sheng YueCui-Cui LiuChen-Guang LiChen ChenHua ZhangHai-Lin LiuZhen-Fa ZhangLiang ChenBin ZhangChang-Li WangPublished in: Cancer science (2021)
Reliable and noninvasive biomarkers for the early diagnosis of non-small-cell lung cancer (NSCLC) are an unmet need. This study aimed to screen and validate potential urinary biomarkers for the early diagnosis of NSCLC. Using protein mass spectrometry, urinary MDH2 was found to be abundant both in patients with lung cancer and lung cancer model mice compared with controls. Urine samples obtained as retrospective and prospective cohorts including 1091 NSCLC patients and 736 healthy controls were measured using ELISA. Patients with stage I NSCLC had higher urinary MDH2 compared with healthy controls. The area under the receiver-operating characteristic curve (AUC) for the urinary MDH2 was 0.7679 and 0.7234 in retrospective and prospective cohorts to distinguish stage I cases from controls. Urinary MDH2 levels correlated with gender and smoking history. MDH2 expression levels were elevated in lung cancer tissues. MDH2 knockdown using shRNA inhibited the proliferation of lung cancer cells. Our study demonstrated that urinary MDH2 concentration was higher in early-stage NSCLC patients compared with that in controls and that MDH2 could serve as a potential biomarker for early detection of NSCLC.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- end stage renal disease
- early stage
- mass spectrometry
- newly diagnosed
- chronic kidney disease
- ejection fraction
- prognostic factors
- gene expression
- mental health
- squamous cell carcinoma
- adipose tissue
- small molecule
- patient reported outcomes
- epidermal growth factor receptor
- insulin resistance
- type diabetes
- high resolution
- climate change
- liquid chromatography
- long non coding rna
- high performance liquid chromatography
- high fat diet induced
- single cell
- tandem mass spectrometry
- tyrosine kinase