“…A number of studies have shown that HOXB7 is abnormally expressed in a variety of solid tumors including oral squamous cell carcinoma (OSCC), colon cancer, breast cancer, esophageal cancer, pancreatic cancer, lung cancer, gastric cancer, and liver cancer [16] . However, the development and outcome of the disease caused by this abnormal expression are not always consistent, which is manifested in: Although most studies have supported the conclusion that abnormally high expression of HOXB7 was related to worse survival of the patients, there are still several studies with different results showing a correlation trend but without statistical significance between high expression of HOXB7 and poorer survival of salivary gland tumor patients, OSCC patients, and gastric cancer patients [17–19] . However, there were some shortcomings in these 3 studies, such as the pathological types were mixed with benign and malignant tumors, which resulted in the different treatment options, most of the included patients were in stage III/IV and insufficient of sample size as well as follow-up time.…”