Therapeutic inhibition of microRNA-21 (miR-21) using locked-nucleic acid (LNA)-anti-miR and its effects on the biological behaviors of melanoma cancer cells in preclinical studies

Long noncoding RNA X-inactive specific transcript promotes malignant melanoma progression and oxaliplatin resistance

(2019) Bujian Pan et al.   MELANOMA RESEARCH

Role of miRNAs in Melanoma Metastasis

(2019) Anna Gajos-Michniewicz et al.   Cancers

Metformin Treatment Suppresses Melanoma Cell Growth and Motility Through Modulation of microRNA Expression

(2019) Hui-Wen Tseng et al.   Cancers

miR-let-7b and miR-let-7c suppress tumourigenesis of human mucosal melanoma and enhance the sensitivity to chemotherapy

(2019) Huan Tang et al.   JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH

Nodal Facilitates Differentiation of Fibroblasts to Cancer-Associated Fibroblasts that Support Tumor Growth in Melanoma and Colorectal Cancer

(2019) Ziqian Li et al.   Cells

microRNA: The Impact on Cancer Stemness and Therapeutic Resistance

(2019) Xueqiao Jiao et al.   Cells

circRNA_0084043 promote malignant melanoma progression via miR-153-3p/Snail axis

(2018) Wenkang Luan et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

The EMT-related transcription factor snail up-regulates FAPα in malignant melanoma cells

(2018) Yanmei Yi et al.   EXPERIMENTAL CELL RESEARCH

Loss of miR-204 expression is a key event in melanoma

(2018) Marco Galasso et al.   Molecular Cancer

Cell death-based treatments of melanoma:conventional treatments and new therapeutic strategies

(2018) Gianfranco Mattia et al.   Cell Death & Disease

Current Status and Perspectives Regarding LNA-Anti-miR Oligonucleotides and microRNA miR-21 Inhibitors as a Potential Therapeutic Option in Treatment of Colorectal Cancer

(2017) Reza Nedaeinia et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Current Status and Prospective Regarding the Therapeutic Potential of Natural Autoantibodies in Cancer Therapy

(2017) Salimeh Ebrahimnezhad et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Identification of microRNAs associated with invasive and aggressive phenotype in cutaneous melanoma by next-generation sequencing

(2017) Sankhiros Babapoor et al.   LABORATORY INVESTIGATION

Inhibition of microRNA-21 via locked nucleic acid-anti-miR suppressed metastatic features of colorectal cancer cells through modulation of programmed cell death 4

(2017) Reza Nedaeinia et al.   TUMOR BIOLOGY

Locked nucleic acid anti-miR-21 inhibits cell growth and invasive behaviors of a colorectal adenocarcinoma cell line: LNA-anti-miR as a novel approach

(2016) R Nedaeinia et al.   CANCER GENE THERAPY

Circulating exosomes and exosomal microRNAs as biomarkers in gastrointestinal cancer

(2016) R Nedaeinia et al.   CANCER GENE THERAPY

BRAF and epithelial-mesenchymal transition in primary cutaneous melanoma: a role for Snail and E-cadherin?

(2016) Brendon Mitchell et al.   HUMAN PATHOLOGY

C-myc overexpression drives melanoma metastasis by promoting vasculogenic mimicry via c-myc/snail/Bax signaling

(2016) Xian Lin et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Lumican Inhibits SNAIL-Induced Melanoma Cell Migration Specifically by Blocking MMP-14 Activity

(2016) Marta Stasiak et al.   PLoS One

Metastatic Melanoma – A Review of Current and Future Treatment Options

(2015) E Maverakis et al.   ACTA DERMATO-VENEREOLOGICA

miR networks in melanoma - more to come!

(2013) Silke Kuphal et al.   Pigment Cell & Melanoma Research

Differential Stability of Cell-Free Circulating microRNAs: Implications for Their Utilization as Biomarkers

(2013) Verena Köberle et al.   PLoS One

Convergent Multi-miRNA Targeting of ApoE Drives LRP1/LRP8-Dependent Melanoma Metastasis and Angiogenesis

(2012) Nora Pencheva et al.   CELL

The ethyl acetate extract of PGP (Phellinus linteus grown on Panax ginseng) suppresses B16F10 melanoma cell proliferation through inducing cellular differentiation and apoptosis

(2010) Hye-Jin Park et al.   JOURNAL OF ETHNOPHARMACOLOGY

MicroRNA-21 targets tumor suppressor genes in invasion and metastasis

(2008) Shuomin Zhu et al.   CELL RESEARCH