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. 2020 Jul 9;5(3):109–115. doi: 10.1016/j.ncrna.2020.06.003

Table 3.

Summary of studies reported expression of TINCR in clinical samples (Gastrointestinal stromal tumors (GIST), Head and neck Squamous cell carcinoma (HNSCC), Disease free survival (DFS), overall survival (OS)).

Cancer type Numbers of clinical samples (tissues, serum, etc.) Expression (Tumor vs. Normal) Kaplan-Meier analysis Univariate cox regression Multivariate cox regression Reference
Gastric cancer (GC) 80 primary GC tissue samples and paired adjacent non-tumor tissue samples Up The high TINCR patients had higher recurrence rates than the low-TINCR patients. TINCR expression was a significant prognostic indicator of DFS in patients with GC TINCR expression was a significant prognostic indicator of DFS in patients with GC [6]
Plasma samples from 162 patients with GC, 110 healthy controls, 28 patients with precancerous lesions and 21 with GIST Up [10]
56 primary GC tissue samples and paired adjacent non-tumor tissue samples Up [4]
Colorectal cancer 80 pairs of CRC tissues and adjacent non-tumor tissues, 80 CRC plasma and 80 normal control Up High expression of TINCR predicted a poor OS (p < 0.001). High expression of TINCR was predictors for poor OS. High expression of TINCR was an independent predictor of poor OS. [12]
44 CRC tissues and their paired normal colorectal mucosa Down [7]
Esophageal squamous cell carcinoma (ESCC) 56 pairs of primary ESCC tissues and adjacent normal tissues Up [22]
Squamous cell carcinoma (SCC) TCGA cohort of HNSCC patients Down Low levels of TINCR were significantly correlated with poor outcome of patients with HNSCC. [24]
Oral squamous cell carcinoma (OSCC) 48 pairs of primary OSCC tissues and adjacent normal tissues Up Patients with high TINCR had reduced OS and progressive-free survival rates, compared with patients with low expression of this lncRNA. [23]
Non-small cell lung cancer 98 pairs of NSCLC tissues and normal adjacent tissues Up High TINCR expression was correlated with poor survival. [14]
37 pairs of NSCLC tissues and normal adjacent tissues Up [28]
70 pairs of NSCLC tissues and normal adjacent tissues Down Patients with low TINCR levels in NSCLC tissues had much worse survival rate. [15]
Lung cancer 45 cases of lung cancer tumor tissues and adjacent normal tissues Down [29]
Hepatocellular carcinoma (HCC) 248 pairs of HCC tissues and normal adjacent tissues Up Patients with high TINCR expression tended to have worse DFS and OS. TINCR was an independent poor prognostic indicator for DFS and OS in HCC. [30]
66 pairs of HCC tissues and normal adjacent tissues Down Low TINCR levels in HCC tissues were associated with low 5-year OS. [16]
60 pairs of HCC tissues and normal adjacent tissues Up [18]
56 pairs of HCC tumor tissues and adjacent normal liver tissues Up High TINCR expression was correlated with worse OS. [18]
Glioma 61 pairs of glioma tissues and normal adjacent tissues Down [25]
Breast cancer 26 GEO datasets with 4140 breast cancer including patients' long-term follow-up information Up High TINCR expression was correlated with worse OS. [20]
24 cases of breast cancer tumor tissues and adjacent normal tissues Up High TINCR expression was correlated with worse prognosis. [19]
60 patients with HER-2+ breast cancer who underwent surgical resection followed by trastuzumab treatment and primary cancer tissues before performing trastuzumab treatment Up High TINCR expression was associated with poor survival in patients receiving trastuzumab therapy. [21]
Prostate cancer 52 pairs of normal prostatic tissues and prostate cancer tissues from TCGA database, Fresh 160 prostate cancer tissue specimens and 30 paired normal prostatic tissue specimens from 160 patients Down Level of TINCR is positively correlated with the OS of prostate cancer cases. TINCR low expression was an unfavorable prognostic factor for prostate cancer patients. [5]
Bladder cancer (BCa) 49 paired BCa tissues and corresponding noncancerous tissues Up [31]
Retinoblastoma (RB) 60 pairs of RB tissues and normal adjacent tissues Down [26]