lung cancer gene and literature database Home
Cancer metastasis database

Annotation category 5

Literatures

Literature evidence

Links to all GeneRIF Items

8140

PubMed (Gene Name)

Literature evidence

18253116 (SLC7A5)

Overexpression of L-type amino acid transporter 1 is associated with nonsmall cell lung cancer

19068093 (SLC7A5)

Elevated expression of CD98 is associated with squamous cell carcinoma of the lung.

19171406 (SLC7A5)

over expression of Lat1 is a pathological factor to predict the prognosis in patients with resectable stage I pulmonary adenocarcinoma

19430419 (SLC7A5)

the percentage of lung carcinoma patients remaining unclassifiable by TTF-1/TP63 was twice that of the five-antibody (TRIM29, CEACAM5, SLC7A5, MUC1, and CK5/6) test

19559497 (SLC7A5)

higher mRNA levels in non-small-cell lung carcinomas compared to normal lung tissues

19635099 (SLC7A5)

Multivariate analysis confirmed that positive expression of LAT1 was an independent factor for predicting a poor prognosis in surgically resected stage I non-small cell lung cancer.

19777189 (SLC7A5)

High LAT1 expression is associated with non-small-cell lung cancer with lymph node metastases.

21055621 (SLC7A5)

LAT1 expression is a stronger prognostic factor than (18)F-FAMT uptake in surgically resected non-small cell lung cancer

22110199 (SLC7A5)

High LAT1 expression is associated with drug resistance in non-small cell lung cancer.

27566573 (SLC7A5)

LAT1-NAD+-SIRT1 signaling is activated in tumor tissues of patients with non-small cell lung cancer; NAD+ synthesis regulates the SIRT1-FOXO1 apoptotic pathway in response to NQO1

29277611 (SLC7A5)

Thus, our results indicated that lncRNA-PVT1-5 may function as a competing endogenous RNA (ceRNA) for miR-126 to promote cell proliferation by regulating the miR-126/SLC7A5 pathway, suggesting that lncRNA-PVT1-5 plays a crucial role in lung cancer progression and lncRNA-PVT1-5/miR-126/SLC7A5 regulatory network may shed light on tumorigenesis in lung cancer.

29326164 (SLC7A5)

Data suggest that amino acid uptake via ASCT2/SLC1A5 is required for cell proliferation/tumor growth independently of LAT1/SLC7A5; in part, these studies were conducted in lung and colon adenocarcinoma cell lines and involved gene knockout techniques. (ASCT2/SLC1A5 = solute carrier family-1 member-5; LAT1/SLC7A5 = solute carrier family-7 member-5)

30300664 (SLC7A5)

LAT1 and 4F2hc were identified as significant independent markers for predicting a worse prognosis in patients with pulmonary pleomorphic carcinoma

30528230 (SLC7A5)

Dysfunction of MINCR, miR-126 and SLC7A5 predicted poor prognosis of patients with non-small cell lung cancer.