Page 54 - GPD-1-2
P. 54

Gene & Protein in Disease                                                         circRNAs and cancer
































            Figure 1. Orientation of circRNAs as a diagnostic biomarker for cancers through liquid biopsy. Using body fluids and other molecular biomarkers, effective
            management strategies for cancer diagnostic screening. The body fluids of cancer patients contain disease-specific circulating free DNA/RNA, circRNAs,
            and circulating tumor cells. Various molecular biology techniques, such as digital droplet PCR, NanoString technology, microarrays, and next-generation
            sequencing, can be used to analyze the nucleic acid extracted from a sample of body fluids.

            EMT,  drug  transport and  metabolism,  autophagy,  and   three-dimensional cellular systems as research platforms.
            apoptosis inhibition enhance drug resistance [154] . CircRNAs   Due  to  their  ability  to faithfully  mimic  the  evolution
            interact with these molecules and modify them to promote   of cancer, inducible systems that overexpress genes are
            drug resistance [155] .                            valuable models for observing circRNA expression and
                                                               changes during tumor progression in two-dimensional
              Various drug response pathways, such as PI3K/                   [159]
            AKT,  MAPK,  VEGFR,  MEK/ERK,  and the ATP-        biological systems  . In addition, to gain crucial
            binding cassette (ABC) transport system, are regulated   knowledge about the pathways and processes impacted
            by circRNAs as well [156] . According to a recent study,   by circRNA entities, it is possible to experimentally assess
            circNFIX was  overexpressed in  temozolomide-resistant   the impact of circRNAs’ potential qualitative/quantitative
                                                               variations on other properties, such as RBPs and miRNAs.
            glioma individuals and conferred temozolomide resistance   Similarly, three-dimensional cellular systems, including
            to recipient glioma cells through exosomes through   brain organoids made from iPSCs [159] , have already been
            inhibiting  miR-132 [151] .  CircPVT1 promotes treatment   used in circRNA research. About 56% of the detected
            resistance to doxorubicin and cisplatin in osteosarcoma
            tissues, blood, and chemoresistant cell lines by increasing   circRNAs in those organoid cultures overlapped circRNAs
                                                               from the postmortem brain
                                                                                        . The highest in terms of
                                                                                      [160]
            the expression of the  ABCB1 gene [157] . Furthermore,   ability and similarity to the original tissue are patient-
            through the miR-182-5p/FOXO3a axis, hsa_circ_0025202   derived organoids, indicating their broad applications
            overexpression is frequently downregulated in BC tissues   in  various  malignancies,  including  GC [161-166] .  Other
            and tamoxifen-resistant cell lines, reduces cell division and   approaches for studying circRNAs include animal
            movement, boosts cell apoptosis, and improves tamoxifen   models with manipulable loci encoding these molecules.
            sensitivity [158] . The above findings suggest that circRNAs   Sensorimotor gating was disturbed in mice with a
            perform a vital part in chemoresistance. Figure 2 depicts   deletion in the Cdr1 as circRNA gene, which substantially
            certain anticancer drug-resistant circRNAs in various   binds  miR-7 and  miR-671, leading in neuropsychiatric
            malignancies.                                      problems due to the animals’ inability to filter out
            5. Implementation of new models in circRNA         redundant data [165] . In addition, a study utilized shRNAs
            cancer research                                    to selectively downregulate five highly expressed circRNAs
                                                               in Drosophila by targeting particular circRNA-back-splice
            The significance of circRNAs in the pathophysiology of   junctions [166] .  The  downregulation  of  circ–Ctrip  resulted
            specific cells is being studied using two-dimensional and   in developmental lethality. These examples highlight


            Volume 1 Issue 2 (2022)                         7                      https://doi.org/10.36922/gpd.v1i2.138
   49   50   51   52   53   54   55   56   57   58   59