Journal: Journal of Cancer

Article Title: mRNA Expression of FGFR1 as Potential Marker for Predicting Prognosis of Surgical Resection of Small Cell Lung Cancer may be better than Protein Expression and Gene Amplification

doi: 10.7150/jca.44476

Figure Lengend Snippet: Diagrammatic representation of FGFR1 mutation from www.cbioportal.org .

Article Snippet: IHC for FGFR1 was performed using FGFR1 antibody (Cat, #BA0485, Boster Biological Technology Co. Ltd).

Techniques: Mutagenesis

Journal: Journal of Cancer

Article Title: mRNA Expression of FGFR1 as Potential Marker for Predicting Prognosis of Surgical Resection of Small Cell Lung Cancer may be better than Protein Expression and Gene Amplification

doi: 10.7150/jca.44476

Figure Lengend Snippet: FGFR1 protein expression by immunohistochemistry in SCLC and their correlations with prognosis. (A ) shows FGFR1 protein positive expression; ( B ) shows FGFR1 protein negative expression. Kaplan-Meier Survival analysis of FGFR1 protein-positive vs. FGFR1 protein-negative ( C and D ).

Article Snippet: IHC for FGFR1 was performed using FGFR1 antibody (Cat, #BA0485, Boster Biological Technology Co. Ltd).

Techniques: Expressing, Immunohistochemistry

Journal: Journal of Cancer

Article Title: mRNA Expression of FGFR1 as Potential Marker for Predicting Prognosis of Surgical Resection of Small Cell Lung Cancer may be better than Protein Expression and Gene Amplification

doi: 10.7150/jca.44476

Figure Lengend Snippet: Clinicopathological data of the patients with SCLC and FGFR1 status

Article Snippet: IHC for FGFR1 was performed using FGFR1 antibody (Cat, #BA0485, Boster Biological Technology Co. Ltd).

Techniques: Amplification

Journal: Journal of Cancer

Article Title: mRNA Expression of FGFR1 as Potential Marker for Predicting Prognosis of Surgical Resection of Small Cell Lung Cancer may be better than Protein Expression and Gene Amplification

doi: 10.7150/jca.44476

Figure Lengend Snippet: FGFR1 amplification by fluorescence in situ hybridization in SCLC and their correlations with prognosis. ( A ) shows FGFR1 amplification ( B ) shows FGFR1 non-amplification. Kaplan-Meier Survival analysis of FGFR1 amplified vs. non-amplified tumors ( C and D ).

Article Snippet: IHC for FGFR1 was performed using FGFR1 antibody (Cat, #BA0485, Boster Biological Technology Co. Ltd).

Techniques: Amplification, Fluorescence, In Situ Hybridization

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Identification of genes discriminating FGFR1 amplification from FGFR1 neutral in the discovery cohort [ie, the preoperative letrozole (POL)-Z1031 cohort]. A: The REMARK diagram shows 25 FGFR1-amplified estrogen receptor–positive (ER+) tumors were chosen to be compared against 39 FGFR1 neutral and chromosome 8 diploid ER+ tumors for genes discriminative of FGFR1 amplification. B: Firestorm analysis. The segmented array comparative genomic hybridization (aCGH) copy number signals from the circular binary segmentation algorithm (in log2 ratio, y axis) were plotted against chromosome 8 genome locations (x axis). The top panel shows a FGFR1 firestorm amplified tumor example, and the bottom panel shows a FGFR1 neutral and chromosome 8 diploid tumor example. C: Heat map of the mRNA gene expression levels (in red/green color scheme) of the nine genes (at row). Overexpression of the genes corresponds well to the FGFR1-amplified cases among the 64 samples (at column), as determined by the firestorm analysis (indicated in the top image bar as truth: AMP in pink for amplification and NonAMP in blue for nonamplification).

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Amplification, Hybridization, Gene Expression, Over Expression

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Validation of individual genes and development/evaluation of multigene signatures in the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) cohort. A: The REMARK diagram; 1508 estrogen receptor–positive (ER+) METABRIC samples were used for FGFR1 amplification analyses. B: Disease-specific survival (DSS) Kaplan-Meier (KM) curves of true FGFR1 amplification status, as determined by single-nucleotide polymorphism (SNP) array copy number analysis stratified by ER status, demonstrated that FGFR1 amplification is prognostic in ER+ tumors but not in ER- tumors. In parentheses are total number of events/total number of samples with valid survival and FGFR1 amplification data. The hazard ratios (HRs) with associated 95% CIs and the log-rank test P values (P) are reported. C: Individual receiver operating characteristic (ROC) curve confirms the discriminative ability of each individual gene for FGFR1 amplification. The solid black point indicates the optimal cutoff point on each ROC curve. The legend shows area under the ROC curve (AUC), sensitivity, and specificity corresponding to the optimal cutoff. D: Overlaid KM curves for DSS indicate that each of the four composite signatures is prognostic and tracks the true nonamplified curve well. KM curves of amplification statuses, as determined by each of the four multigene signatures from 10-fold cross-validations (red dashed curves: upper/lower red curves for nonamplified/amplified patients, respectively), were overlaid by gold standard FGFR1 amplification status, as determined by SNP array copy number analysis (black solid curves, upper/lower curves for nonamplified/amplified patients, respectively), and amplification status, as determined by both a signature and the true status (green dotted curves, upper/lower curve for nonamplified cases determined by both/amplified cases determined by both, respectively). The HRs with associated 95% CIs and the log-rank test P values (P) are reported. The signature Call-FGFR1-amp based on the optimal AUC (optAUC) algorithm was carried forward locked down for validation. EMP, empirical method; Logistic, logistic regression method; NB, naïve Bayes method.

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Biomarker Discovery, Amplification

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Validation of FGFR1 amplification calls by Call-FGFR1-amp in the Strategic Partnering to Evaluate Cancer Signatures (SPECS) cohort. A: The REMARK diagram; 47 estrogen receptor–positive (ER+) SPECS samples were analyzed for FGFR1 amplification analyses. B: Kaplan-Meier (KM) curves by true FGFR1 amplification status, as determined by fluorescent in situ hybridization (FISH) for relapse-free survival (RFS), overall survival (OS), and disease-specific survival (DSS), show prognostic trends. Indicated in the legend are the total number of events/total number of patients corresponding to the amplified and nonamplified patients in the parenthesis, hazard ratios (HRs), and 95% CIs and log-rank test P values (P). C: Heat map of the nine selected genes (at row) shows concordance between the genes' overexpression, the amplification statuses called by Call-FGFR1-amp, and the FGFR1 FISH amplification statuses of the 47 ER+ tumors (at column), indicated in the top image bar by pred (for Call-FGFR1-amp) and truth (for FISH), respectively. AMP in pink/purple for amplification and NonAMP in blue for nonamplification. White bars are for cases with nonreadable FISH results. D: Overlaid KM curves exhibit close tracking of Call-FGFR1-amp for FGFR1 FISH, showing similar prognostic effects. KM curves for RFS, OS, and DSS by FGFR1 amplification based on Call-FGFR1-amp (Call-FGFR1-amp: red dashed curves, upper/lower red curves corresponding to nonamplified versus amplified patients, as determined by Call-FGFR1-amp, respectively), overlaid with curves by the FISH gold standard (FGFR1: black solid curves, upper/lower curves corresponding to nonamplified versus amplified patients, as determined by FISH, respectively) and FGFR1 status, as determined by both Call-FGFR1-amp and FISH (FGFR1 and Call-FGFR1-amp: green dotted curves, the upper green dotted curve representing patients who were FGFR1 FISH amplified and called so by Call-FGFR1-amp versus the lower green dotted curves representing the remaining patients who were called nonamplified by both or had inconsistent calls between FISH and Call-FGFR1-amp). The HRs with 95% CIs and log-rank test P values (P) were indicated in the legend.

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Biomarker Discovery, Amplification, In Situ Hybridization, Over Expression

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Validation of FGFR1 amplification calls by Call-FGFR1-amp in the University of British Columbia (UBC)–tamoxifen (TAM) cohort. A: The REMARK diagram; 651 estrogen receptor–positive (ER+) UBC-TAM samples were analyzed for FGFR1 amplification analyses. B: Kaplan-Meier (KM) curves by true FGFR1 amplification status, as determined by fluorescent in situ hybridization (FISH), show prognostic effects for disease-specific survival (DSS) and relapse-free survival (RFS). C: Heat map of the nine selected genes (at row) shows concordance between the genes' overexpression, the amplification statuses called by Call-FGFR1-amp, and the FGFR1 FISH amplification statuses of the 651 ER+ tumors (at column), indicated in the top image bar by pred (for Call-FGFR1-amp) and truth (for FISH), respectively. AMP in pink/purple for amplification and NonAMP in blue for nonamplification. White bars are for cases with nonreadable FISH results. D: Overlaid KM curves exhibit close tracking of Call-FGFR1-amp for FGFR1 FISH, showing similar prognostic effects. KM curves for DSS and RFS by FGFR1 amplification based on Call-FGFR1-amp (Call-FGFR1-amp: red dashed curves, upper/lower red curves corresponding to nonamplified versus amplified patients, as determined by Call-FGFR1-amp, respectively), overlaid with curves by the FISH gold standard (FGFR1: black solid curves, upper/lower curves corresponding to nonamplified versus amplified patients, as determined by FISH, respectively) and FGFR1 status, as determined by both Call-FGFR1-amp and FISH (FGFR1 and Call-FGFR1-amp: green dotted curves, the upper green dotted curve representing patients who were FGFR1 FISH amplified and called so by Call-FGFR1-amp versus the lower green dotted curves representing the remaining patients who were called nonamplified by both or had inconsistent calls between FISH and Call-FGFR1-amp). The hazard ratios (HRs) with 95% CIs and log-rank test P values (P) were indicated in the legend. QC, quality control.

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Biomarker Discovery, Amplification, In Situ Hybridization, Over Expression, Control

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Selection of the Candidate Genes in the Discovery Cohort (POL-Z1031)

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Selection

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Contingency Table of FGFR1 Amplification Calls as Determined by Call-FGFR1-amp against the FISH Gold Standards in the SPECS Cohort

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Amplification

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: An mRNA Gene Expression–Based Signature to Identify FGFR1 -Amplified Estrogen Receptor–Positive Breast Tumors

doi: 10.1016/j.jmoldx.2016.09.007

Figure Lengend Snippet: Contingency Table of FGFR1 Amplification Calls as Determined by Call- FGFR1 -Amp against the FISH Gold Standards in the UBC-TAM Cohort

Article Snippet: FGFR1 (8p12)/CEN8q FISH probes (Abnova, Taipei, Taiwan) were codenatured with the tissues at 73°C for 5 minutes and hybridized at 37°C for 16 to 18 hours.

Techniques: Amplification