The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays
Open accessAbstract
To identify genomic abnormalities characteristic of pancreatic ductal adenocarcinoma (PDAC) in vivo, a panel of 27 microdissected PDAC specimens were analysed using high-density microarrays representing approximately 116 000 single nucleotide polymorphism (SNP) loci. We detected frequent gains of 1q, 2, 3, 5, 7p, 8q, 11, 14q and 17q (> or =78% of cases), and losses of 1p, 3p, 6, 9p, 13q, 14q, 17p and 18q (> or =44%). Although the results were comparable with those from array CGH, regions of those genetic changes were defined more accurately by SNP arrays. Integrating the Ensembl public data, we have generated 'gene' copy number indices that facilitate the search for novel candidates involved in pancreatic carcinogenesis. Copy numbers in a subset of the genes were validated using quantitative real-time PCR. The SKAP2/SCAP2 gene (7p15.2), which belongs to the src family kinases, was most frequently (63%) amplified in our sample set and its recurrent overexpression (67%) was confirmed by reverse transcription-PCR. Furthermore, fluorescence in situ hybridization and in situ RNA hybridization analyses for this gene have demonstrated a significant correlation between DNA copy number and mRNA expression level in an independent sample set (P<0.001). These findings indicate that the dysregulation of SKAP2/SCAP2, which is mostly caused by its increased gene copy number, is likely to be associated with the development of PDAC.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In this “pseudo-bulk” summary, previously described hallmark genomic events characteristic of PDAC lesions1–6 were readily observed, albeit in some cases only in a subset of genomic subclones for each line.”
From Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolution (2022) · cites this paper as [3]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Spencer, P. M., Cameron, J. L., & Lin, L. (2000) · Cited by 7,202
Global variation in copy number in the human genome
Redon, R., Ishikawa, S., Fitch, K. R., Feuk, L., Perry, G. H., Andrews, T. D., Fiegler, H., Shapero, M. H., Carson, A. R., Chen, W., et al. (2006) · Nature · doi:10.1038/nature05329 · Cited by 4,377 · cited 2×
“Taking structural variation in the human genome into account, our software integrated the public data of CNVs (http://projects. tcag.ca/variation/) into our analysis (Iafrate et al., 2004; Redon et al., 2006).”
BackgroundMethodJemal, A., Murray, T., Ward, E., Samuels, A., Tiwari, R. C., Ghafoor, A., Feuer, E. J., & Thun, M. J. (2005) · CA: A Cancer Journal for Clinicians · doi:10.3322/canjclin.55.1.10 · Cited by 4,186 · cited 2×
“Essentially, no conventional treatment has made a significant impact on the course of the disease, so that the prognosis for patients still remains dismal with a median survival of approximately 6 months from diagnosis and an overall 5-year survival of less than 5% (Jemal et al., 2005).”
BackgroundDetection of large-scale variation in the human genome
Iafrate, A. J., Feuk, L., Rivera, M. N., Listewnik, M. L., Donahoe, P. K., Qi, Y., Scherer, S. W., & Lee, C. (2004) · Nature Genetics · doi:10.1038/ng1416 · Cited by 2,892 · cited 1×
“Taking structural variation in the human genome into account, our software integrated the public data of CNVs (http://projects. tcag.ca/variation/) into our analysis (Iafrate et al., 2004; Redon et al., 2006).”
MethodLi, D., Xie, K., Wolff, R. A., & Abbruzzese, J. L. (2004) · The Lancet · doi:10.1016/s0140-6736(04)15841-8 · Cited by 1,731 · cited 2×
“Thus, recurrent genetic changes that were previously characterized in PDAC were commonly observed in our analysis (Bardeesy and DePinho, 2002; Li et al., 2004).”
BackgroundResultGenomic and transcriptional aberrations linked to breast cancer pathophysiologies
Chin, K., DeVries, S., Fridlyand, J., Spellman, P. T., Roydasgupta, R., Kuo, W.-L., Lapuk, A. V., Neve, R. M., Qian, Z., Ryder, T., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.10.009 · Cited by 1,309
Pancreatic cancer biology and genetics
Bardeesy, N. M., & DePinho, R. A. (2002) · Nature reviews. Cancer · doi:10.1038/nrc949 · Cited by 1,176
The role of focal-adhesion kinase in cancer — a new therapeutic opportunity
McLean, G. W., Carragher, N. O., Avizienyte, E., EVANS, J., Brunton, V. G., & Frame, M. C. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1647 · Cited by 1,049 · cited 1×
“However, based on the ability of SCAP2 to interact with RAFTK, it is likely to modulate the spreading and motility of PDAC cells (McLean et al., 2005).”
BackgroundNannya, Y., Sanada, M., Nakazaki, K., Hosoya, N., Wang, L., Hangaishi, A., Kurokawa, M., Chiba, S., Bailey, D. K., Kennedy, G. C., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-0465 · Cited by 632 · cited 1×
“0) software (http://www.genome.umin.jp/) (Nannya et al., 2005).”
Zhao, X. J., Li, C., Paez, J. G., Chin, K., Janne, P. A., Chen, T.-H., Girard, L., Minna, J. D., Christiani, D. C., Leo, C., et al. (2004) · Cancer Research · doi:10.1158/0008-5472.can-03-3308 · Cited by 543 · cited 4×
“…arrays has allowed genome-wide, high-resolution analysis of both DNA copy number (DCN) alterations and loss of heterozygosity (LOH) events in cancer cells (Lindblad-Toh et al., 2000; Bignell et al., 2004; Huang et al., 2004; Janne et al., 2004; Zhao et al., 2004, 2005; Midorikawa et al., 2006).”
BackgroundMethodInfluential
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–159 of 159
Andrieux, J., & Sheth, F. J. (2009) · PubMed · Cited by 9
Sleptcov, A. A., Nazarenko, M. S., Лебедев, И. Н., Skryabin, N. A., Frolov, A. V., Va, P., Барбараш, О. Л., Barbarash, L. S., & Puzyrev, V. P. (2014) · Russian Journal of Genetics · doi:10.1134/s1022795414080080 · Cited by 9
Puces à ADN (CGH-array) : application pour le diagnostic de déséquilibres cytogénétiques cryptiques
Andrieux, J. (2008) · Pathologie Biologie · doi:10.1016/j.patbio.2008.04.011 · Cited by 9
Fast MCMC sampling for hidden markov models to determine copy number variations
Mahmud, M. P., & Schliep, A. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-428 · Cited by 9
“Finally, we report findings from an analysis of Mantle Cell Lymphoma (MCL) cell lines [29], Corriel cell lines [30], GBM datasets [31], and high resolution SNP arrays [13,32].”
BackgroundMethodInfluentialCoenen, M. J. H., Ploeg, M., Schijvenaars, M. M. V. A. P., Cornel, E. B., Karthaus, H. F. M., Scheffer, H., Witjes, J. A., Franke, B., & Kiemeney, L. A. L. M. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-1103 · Cited by 8
Wang, Z., Han, H., Zhang, C., Wu, C., Di, J., Xing, P., Qiao, X., Weng, K., Hao, H., Yang, X., et al. (2024) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-024-03193-7 · Cited by 8
Legoffic, A., Calvo, E. L., Barthet, M. A., Delpéro, J., Dagorn, J. C., & Iovanna, J. (2009) · Pancreatology · doi:10.1159/000212092 · Cited by 7
Brucker, A., Lu, W., West, R. M., Yu, Q.-Y., Hsiao, C. K., Hsiao, T.-H., Lin, C., Magnusson, P. K. E., Sullivan, P. F., Szatkiewicz, J., et al. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007797 · Cited by 7
Differential Diagnosis of Pancreatic Tumors by Molecular Analysis of Clinical Specimens
Buchholz, M., Kestler, H. A., & Gress, T. M. (2008) · Pancreatology · doi:10.1159/000159213 · Cited by 7
Fan, Z., Zhou, J., Tian, Y., Yu, Q., Liu, Z., Gu, L., Dawsey, S. M., Wei, W., & Deng, D. (2024) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002982 · Cited by 6
Copy number variation at 6q13 is associated with lung cancer risk in a Han Chinese population
Hu, X.-Y., Bai, X., Qiao, X., & Zhu, Y. (2013) · Experimental Lung Research · doi:10.3109/01902148.2013.822946 · Cited by 6
Muñoz‐Minjares, J., & Shmaliy, Y. S. (2016) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2016.08.009 · Cited by 6
Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolution
Monberg, M. E., Geiger, H. M., Lee, J. J., Sharma, R., Semaan, A., Bernard, V., Wong, J., Wang, F., Liang, S., Swartzlander, D. B., et al. (2022) · RePEc: Research Papers in Economics · Cited by 6
English, I. A., Worth, P. J., Hawthorne, K., Vergara, M., Pelz, K. R., Kiemen, A. L., Shah, V., Blise, K. E., Pelz, C., Tsuda, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.14.664767 · Cited by 6
Gutiérrez, M. L., Muñoz‐Bellvís, L., Sarasquete, M. E., Hernández, D. G., Abad, M., Bengoechea, Ó., Corchete, L. A., González‐González, M., García-García, J., González, M., et al. (2014) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2014.06.007 · Cited by 4
Asting, A. G., Ljungman, D., Carén, H., Dambrauskas, Ž., Iresjö, B., Hyltander, A. G., Naredi, P. L. J., & Lundholm, K. (2015) · Pancreas · doi:10.1097/mpa.0000000000000566 · Cited by 3
Neumann-Mufweba, A., Kimani, S., Khan, S. F., Chibale, K., & Prince, S. (2021) · EXCLI journal · doi:10.17179/excli2021-4323 · Cited by 3
Validation of a targeted next-generation sequencing panel for pancreatic ductal adenocarcinomas
Racu, M.-L., Schiavo, A. A., Campenhout, C. V., Nève, N. D., Masuy, T., Maris, C., Decaestecker, C., Remmelink, M., Salmon, I. J., & D’Haene, N. (2024) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2024.104920 · Cited by 3
Pancreatic Cancer: Molecular Genetics and Clinical Applications
Sakorafas, G. H., Pappa, I., & Smyrniotis, V. E. (2010) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0006057.pub2 · Cited by 3
Danesino, C., Biglioli, F., Moneghini, L., Valli, R., Olivieri, C., Testa, B., Baldo, C., Malacarne, M., & Guala, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910664 · Cited by 2
“2, both in the PB and tumor sample, which contains part of a gene, SKAP2 , whose increased copy number is associated with the development of a different type of cancer [24].”
BackgroundScarpa, A., Capelli, P., & Cataldo, I. (2010) · Medical radiology · doi:10.1007/174_2010_4 · Cited by 2
Legrès, L., Janin, A., Masselon, C., & Bertheau, P. (2014) · Cited by 2
Li, X. (2009) · Deep Blue (University of Michigan) · Cited by 2
Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolutionPreprint
Monberg, M. E., Geiger, H., Lee, J. J., Sharma, R., Semaan, A., Bernard, V., Swartzlander, D. B., Stephens, B. M., Chen, K., Katz, M. H., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.13.439717 · Cited by 2
Evidence that extra copies of chromosome 1q play a role in the early phases of pancreatic neoplasia
Douville, C. B., Parksong, J., Molin, M. D., Graham, S., Greipp, P. T., Knudson, R. A., Curtis, S. D., Wang, Y., Dobbyn, L., Popoli, M., et al. (2026) · Science Advances · doi:10.1126/sciadv.adx7501 · Cited by 1
“2 , proposing it as a candidate oncogene ( 49 ).”
Genetically Engineered Mouse Models of Pancreatic Ductal Adenocarcinoma
Hezel, A. F., & Bardeesy, N. M. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-968-0_16 · Cited by 1
Principe et applications de la microdissection laser en histopathologie
Legrès, L., Varna, M., Bouhidel, F. A., Lebœuf, C., Ratajczak, P., Martin, N., Plassa, L., Soliman, H. R., Turpin, E., Lehmann‐Che, J., et al. (2010) · Revue Francophone des Laboratoires · doi:10.1016/s1773-035x(10)70347-6 · Cited by 1
Corbo, V., Mafficini, A., Amato, E., & Scarpa, A. (2012) · Springer eBooks · doi:10.1007/978-94-007-5842-1_8 · Cited by 1
Chromosome 9p21.3 Coordinates Cell Intrinsic and Extrinsic Tumor SuppressionPreprint
Barriga, F. M., Tsanov, K. M., Ho, Y.-J., Sohail, N., Zhang, A. X. W., Baslan, T., Wuest, A. N., Priore, I. S. D., Meškauskaitė, B., Livshits, G., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.22.504793 · Cited by 1
GENOMIC AND TRANSCRIPTOME PROFILING OF EPITHELIAL OVARIAN CANCER
Menzies, R. J., Bukhman, Y. V., Ng, N. F. L., Shaw, P. A., & Mak, T. W. (2008) · Clinical and investigative medicine · doi:10.25011/cim.v31i4.4817
An Integrated Systems Approach to the Study of Pancreatic Cancer
Gadaleta, E., Cutts, R. J., Sangaralingam, A., Lemoine, N. R., & Chelala, C. (2012) · Springer eBooks · doi:10.1007/978-94-007-4819-4_4
Self-citationTang, C., & Lucito, R. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1160-5_7
Med29 Possesses a Complex Role in Pancreatic Cancer
Kuuselo, R. (2010) · Tampere University Institutional Repository (Tampere University)
Reduced representations for efficient analysis of genomic data
Mahmud, M. P. (2014) · doi:10.7282/t3vm49zv
Baumgart, M. (2010) · Kobra (Universitätsbibliothek Kassel)
Current state of the evolving MMMN cancer progression models of cancer
Thiagalingam, S. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9780511979811.022
Strategies to Target Pancreatic Cancer
Liou, G., & Störz, P. (2016) · Springer eBooks · doi:10.1007/978-3-319-31254-5_1
Al-Sukhni, W. (2012) · TSpace (University of Toronto)
Neoplasia of the Gastrointestinal Tract
Margalit, O., & DuBois, R. N. (2015) · Wiley eBooks · doi:10.1002/9781118512074.ch31
Advances in diagnosis of colorectal cancer and pancreatic cancer
Wysocki, P. P., Świętochowska, E., Kiczmer, P., & Ostrowska, Z. (2018) · Pomeranian Journal of Life Sciences · doi:10.21164/pomjlifesci.396
“[22] examined mutations in cancer tissues, mainly chromosome 8q and 9p in 96% (n = 27) and 78% (n = 27) of patients.”
BackgroundTiwari, V. K., & Inayatullah, M. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.739382110.793582242
Cheng, C. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.739382110.793582305
Hahn, W. C. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5847956.5835054
Reinhold, A., & Schraven, B. L. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_629-1
Ivakhno, S., Frese, K. K., Tavaré, S., Iacobuzio–Donahue, C. A., & Tuveson, D. A. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9780511979811.027
Reinhold, A., & Schraven, B. L. (2012) · Springer eBooks · doi:10.1007/978-1-4419-0461-4_629
Reinhold, A., & Schraven, B. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-67199-4_629
Kelber, J. A., Reno, T. A., Kaushal, S., Metildi, C. A., Wright, T. J., Stoletov, K. V., Weems, J. M., Park, F. D., Mose, E. S., Wang, Y., et al. (2023) · doi:10.1158/0008-5472.22390659.v1
Data from Validation of TPX2 as a Potential Therapeutic Target in Pancreatic Cancer Cells
Warner, S. L., Stephens, B. J., Nwokenkwo, S., Hostetter, G. H., Sugeng, A., Hidalgo, M. M., Trent, J. M., Han, H., & Hoff, D. D. V. (2023) · doi:10.1158/1078-0432.c.6517666
Kelber, J. A., Reno, T. A., Kaushal, S., Metildi, C. A., Wright, T. J., Stoletov, K. V., Weems, J. M., Park, F. D., Mose, E. S., Wang, Y., et al. (2023) · doi:10.1158/0008-5472.22390659
Lee, J., Giovannetti, E., Hwang, J., Petrini, I., Wang, Q., Voortman, J., Wang, Y., Steinberg, S. M., Funel, N., Meltzer, P. S., et al. (2023) · doi:10.1158/1078-0432.22444475
Lee, J., Giovannetti, E., Hwang, J., Petrini, I., Wang, Q., Voortman, J., Wang, Y., Steinberg, S. M., Funel, N., Meltzer, P. S., et al. (2023) · doi:10.1158/1078-0432.22444475.v1
Supplementary Methods from Essential Gene Profiles in Breast, Pancreatic, and Ovarian Cancer Cells
Marcotte, R., Brown, K. R., Suárez, F., Sayad, A., Karamboulas, K., Krzyzanowski, P. M., Sircoulomb, F., Medrano, M., Fedyshyn, Y., Koh, J. L. Y., et al. (2023) · doi:10.1158/2159-8290.22529237.v1
Supplementary Methods from Essential Gene Profiles in Breast, Pancreatic, and Ovarian Cancer Cells
Marcotte, R., Brown, K. R., Suárez, F., Sayad, A., Karamboulas, K., Krzyzanowski, P. M., Sircoulomb, F., Medrano, M., Fedyshyn, Y., Koh, J. L. Y., et al. (2023) · doi:10.1158/2159-8290.22529237
Wang, Z., Han, H., Zhang, C., Wu, C., Di, J., Xing, P., Qiao, X., Weng, K., Hao, H., Yang, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.27140773
Ultra-low-pass whole-genome sequencing of bile cfDNA in patients with biliary strictures
Rojo, C., Rullan, M., Sogbe, M., Herranz, J. M., Elizalde, M., Oyón, D., Vila, J. J., Purroy, A., Azkona, M., Marchese, F. P., et al. (2026) · eGastroenterology · doi:10.1136/egastro-2026-100425
“We observed enrichment of 1p losses in PDAC (p=0.046), consistent with prior PDAC copy-number studies, 53 and significantly higher frequencies of 9p losses in CCA (p=0.007; online supplemental table S7).”
InfluentialPaja-García, A., Romero-Becerra, R., Aittokallio, T. A., & Lopez, A. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014735
“17p12 deletion is among the most common losses in PDAC [36], and it has been reported that genetic loss of MAP2K4 gene located in this region occurs in 30% of PDAC cases [36].”
Principles and Applications of Microarray Gene Expression in Pancreatic Cancer
Buchholz, M., & Gress, T. M. (2009) · Springer eBooks · doi:10.1007/978-0-387-77498-5_21
Metadata
- Authors
- Harada, T., Chelala, C., Bhakta, V, Chaplin, T., Caulee, K., Baril, P., Young, B. D., & Lemoine, N. R.
- Affiliations
- University of London (GB)
- Corresponding author
- Lemoine, N R
- Venue
- Oncogene
- Published
- 2007-10-22
- Volume
- 27
- Issue
- 13
- Pages
- 1951-1960
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- PMC
- PMC2492386
- OpenAlex
- W1997162169
- Cited by
- 159
- References
- 34
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 5 · 2023: 9 · 2022: 9 · 2021: 9 · 2020: 5 · 2019: 5 · 2018: 7 · 2017: 4 · 2016: 10 · 2015: 7 · 2014: 8 · 2013: 8 · 2012: 10
- FWCI
- 6.56
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Funders
- Cancer Research UK (A6438, A6789, A6253)
- Topics
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Keywords
- pancreatic ductal adenocarcinoma, DNA copy number alterations, single nucleotide polymorphism array, gene amplification, gene expression, pancreatic carcinogenesis, chromosomal gains and losses
- MeSH terms
- Adenocarcinoma, Adult, Aged, Chromosome Aberrations, Chromosomes, Human, DNA, Neoplasm, Female, Humans, Male, Middle Aged, Nucleic Acid Hybridization, Pancreatic Neoplasms, RNA, Neoplasm, In Situ Hybridization, Fluorescence, Gene Dosage, Loss of Heterozygosity, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Carcinoma, Pancreatic Ductal, Microdissection, Intracellular Signaling Peptides and Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review