circRNA basic information
circBase ID: -
Name: hsa_circ_ZCCHC6
Synonym: circZCCHC6
Host Gene: ZCCHC6
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: extracellular vesicle
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005233
MONDO name: non-small cell lung carcinoma
Disease details: non-small cell lung cancer / NSCLC
Disease DO ID:
3908
Disease MeSH ID:
D002289
Disease NCIt ID:
C2926
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

plasma extracellular vesicle-enriched samples

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: lysophosphatidylcholine acyltransferase 1 (LPCAT1)
Associated microRNA: miR-579-3p, miR-623, miR-1197, miR-1304, miR-548l, miR-605, miR-935
Biological function: -
Molecular mechanism: -
Biological pathway or process:

ceRNA regulation (other)

Detected method:
Q
Validation methods:

RT-qPCR; divergent primers PCR; Back-Splice Junction PCR / divergent primers PCR; Sanger Sequencing; Clinical Sample Validation; Bioinformatics Analysis; ROC Analysis

Clinical significance:

Included in a 10-circRNA signature able to discriminate LC from controls (AUC ROC 0.86).

Description:

circZCCHC6 is up-regulated in plasma EV-enriched samples from early-stage NSCLC patients and was experimentally validated by RT-qPCR with divergent primers and junction confirmation by Sanger sequencing. It is also included in a 10-circRNA machine-learning signature (AUC ROC 0.86) for discriminating NSCLC from controls; the paper notes reported/putative miRNA interactions and a previously described circZCCHC6-miR-433-3p-LPCAT1 regulatory relationship.

Confidence score:

0.6548

Other information
Title:

Multiplex Analysis of CircRNAs from Plasma Extracellular Vesicle-Enriched Samples for the Detection of Early-Stage Non-Small Cell Lung Cancer.

Journal: Pharmaceutics
Published: 2022
PubMed ID: 36297470
Study type:

combined biological and clinical study

Data availability: The data that support the findings of this study are available from the corresponding author (carlospedraz@icloud.com) upon reasonable request.
Code availability: -