CC BY 4.0 · Glob Med Genet 2023; 10(02): 054-062
DOI: 10.1055/s-0043-1768238
Research Article

Replication Timing Aberration of KIF14 and MDM4/PI3KC2β Alleles and Aneuploidy as Markers of Chromosomal Instability and Poor Treatment Response in Ewing Family Tumor Patients

Fernanda Rocha Rojas Ayala
1   Department of Medical Genetics, Unicamp University, Oncogenetics Service at Clinics Hospital, Campinas, SP, Brazil
,
Jeffrey William Martin
2   Department of Medicine, Toronto University, Toronto, Ontario, Canada
,
Carmen Silvia Bertuzzo
3   Department of Genetics and Genomics, at Unicamp University, Oncogenetics Services at Clinics Hospital, Campinas, SP, Brazil
› Author Affiliations
Funding/Acknowledgments Financial support was provided by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Fundação de Apoio à Pesquisa do Estado de São Paulo (FAPESP).

Abstract

Replication timing of allelic gene pairs is strictly regulated according to expression, genome stability, and epigenetic changes, and tumorigenesis may be associated with changes in the allelic replication in various tumors. Our aim was to determine whether such alterations had a prognostic value in Ewing's family tumor (EFT) patients. The KIF14 and MDM4/PI3KC2β and the centromeric satellite sequence of chromosomes 8 and 12 were used for replication timing assessments. Aneuploidy was assessed by enumerating the copy numbers of chromosomes 8 and 12. Replication timing and aneuploidy were detected cytogenetically using multicolors fluorescence in situ hybridization assay applied in 135 EFT. Patients with trisomy 8 presented an association with an asynchronous replication pattern (SD) of MDM4/PI3KC2β genes (p = 0.013). Trisomy 12 was associated with a synchronous pattern (DD) of KIF14 probe signals (p = 0.04). The DD synchronous replication pattern of KIF14 showed a correlation with age (p < 0.0001), and the SS synchronous replication pattern of the same locus showed a correlation with lung metastatic (p = 0.012). The subgroup of patients presenting with multiplet signals of MDM4/PI3KC2β showed an association with treatment response (p = 0.045) and age (p = 0.033). Replication pattern of KIF14 may, significantly, be associated with chromosomal instability as MDM4/PI3KC2β may be a considerably new marker of poor treatment response in EFT patients.



Publication History

Article published online:
21 April 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Gunaratne PH, Nakao M, Ledbetter DH, Sutcliffe JS, Chinault AC. Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region. Genes Dev 1995; 9 (07) 808-820
  • 2 Dotan ZA, Dotan A, Ramon J, Avivi L. Altered mode of allelic replication accompanied by aneuploidy in peripheral blood lymphocytes of prostate cancer patients. Int J Cancer 2004; 111 (01) 60-66
  • 3 Bergman Y, Cedar H. A stepwise epigenetic process controls immunoglobulin allelic exclusion. Nat Rev Immunol 2004; 4 (10) 753-761
  • 4 Gimelbrant AA, Ensminger AW, Qi P, Zucker J, Chess A. Monoallelic expression and asynchronous replication of p120 catenin in mouse and human cells. J Biol Chem 2005; 280 (02) 1354-1359
  • 5 Squire JA, Li M, Perlikowski S. et al. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome. Genomics 2000; 65 (03) 234-242
  • 6 Grinberg-Rashi H, Cytron S, Gelman-Kohan Z, Litmanovitch T, Avivi L. Replication timing aberrations and aneuploidy in peripheral blood lymphocytes of breast cancer patients. Neoplasia 2010; 12 (08) 668-674
  • 7 Amiel A, Levi E, Reish O, Sharony R, Fejgin MD. Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangements. Chromosome Res 2001; 9 (08) 611-616
  • 8 Lengauer C, Kinzler KW, Vogelstein B. Genetic instability in colorectal cancers. Nature 1997; 386 (6625): 623-627
  • 9 Schvartzman JM, Sotillo R, Benezra R. Mitotic chromosomal instability and cancer: mouse modelling of the human disease. Nat Rev Cancer 2010; 10 (02) 102-115
  • 10 Korenstein-Ilan A, Amiel A, Lalezari S, Lishner M, Avivi L. Allele-specific replication associated with aneuploidy in blood cells of patients with hematologic malignancies. Cancer Genet Cytogenet 2002; 139 (02) 97-103
  • 11 Armengol G, Tarkkanen M, Virolainen M. et al. Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization. Br J Cancer 1997; 75 (10) 1403-1409
  • 12 Mugneret F, Lizard S, Aurias A, Turc-Carel C. Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet 1988; 32 (02) 239-245
  • 13 Kullendorff CM, Mertens F, Donnér M, Wiebe T, Akerman M, Mandahl N. Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?. Med Pediatr Oncol 1999; 32 (02) 79-83
  • 14 Zielenska M, Zhang ZM, Ng K. et al. Acquisition of secondary structural chromosomal changes in pediatric Ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome. Cancer 2001; 91 (11) 2156-2164
  • 15 Hattinger CM, Rumpler S, Ambros IM. et al. Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of Ewing tumors. Genes Chromosomes Cancer 1996; 17 (03) 141-150
  • 16 Corson TW, Gallie BL. KIF14 mRNA expression is a predictor of grade and outcome in breast cancer. Int J Cancer 2006; 119 (05) 1088-1094
  • 17 Cahill DP, Lengauer C, Yu J. et al. Mutations of mitotic checkpoint genes in human cancers. Nature 1998; 392 (6673): 300-303
  • 18 Carleton M, Mao M, Biery M. et al. RNA interference-mediated silencing of mitotic kinesin KIF14 disrupts cell cycle progression and induces cytokinesis failure. Mol Cell Biol 2006; 26 (10) 3853-3863
  • 19 Corson TW, Huang A, Tsao MS, Gallie BL. KIF14 is a candidate oncogene in the 1q minimal region of genomic gain in multiple cancers. Oncogene 2005; 24 (30) 4741-4753
  • 20 Abdel-Fatah TM, Powe DG, Agboola J. et al. The biological, clinical and prognostic implications of p53 transcriptional pathways in breast cancers. J Pathol 2010; 220 (04) 419-434
  • 21 Selig S, Okumura K, Ward DC, Cedar H. Delineation of DNA replication time zones by fluorescence in situ hybridization. EMBO J 1992; 11 (03) 1217-1225
  • 22 Haaf T. The effects of 5-azacytidine and 5-azadeoxycytidine on chromosome structure and function: implications for methylation-associated cellular processes. Pharmacol Ther 1995; 65 (01) 19-46 Review
  • 23 Méndez J. Temporal regulation of DNA replication in mammalian cells. Crit Rev Biochem Mol Biol 2009; 44 (05) 343-351 Review
  • 24 Costa CML, Rondinelli P, Campbell B. Tumor neuroectodérmico primitivo da infância: Relato de 13 casos e Revisão de Literatura. J Oncol 2000; 46: 293-298
  • 25 Merscher S, Marondel I, Pedeutour F, Gaudray P, Kucherlapati R, Turc-Carel C. Identification of new translocation breakpoints at 12q13 in lipomas. Genomics 1997; 46 (01) 70-77
  • 26 Sirvent N, Forus A, Lescaut W. et al. Characterization of centromere alterations in liposarcomas. Genes Chromosomes Cancer 2000; 29 (02) 117-129
  • 27 Selvarajah S, Yoshimoto M, Ludkovski O. et al. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH. Cytogenet Genome Res 2008; 122 (01) 5-15
  • 28 Ko E, Rademaker A, Martin R. Microwave decondensation and codenaturation: a new methodology to maximize FISH data from donors with very low concentrations of sperm. Cytogenet Cell Genet 2001; 95 (3-4): 143-145
  • 29 Sugimura H. Detection of chromosome changes in pathology archives: an application of microwave-assisted fluorescence in situ hybridization to human carcinogenesis studies. Carcinogenesis 2008; 29 (04) 681-687 Review
  • 30 Mukherjee AB, Murty VV, Chaganti RS. Detection of cell-cycle stage by fluorescence in situ hybridization: its application in human interphase cytogenetics. Cytogenet Cell Genet 1992; 61 (02) 91-94
  • 31 Böhling T, Bacchini P, Bertoni F. et al. Diagnosis and tumor response in osteosarcoma and Ewing's sarcoma. Acta Orthop Scand Suppl 2004; 75 (311) 72-76
  • 32 Knoll JH, Cheng SD, Lalande M. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region. Nat Genet 1994; 6 (01) 41-46
  • 33 White LM, Rogan PK, Nicholls RD, Wu BL, Korf B, Knoll JH. Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy. Am J Hum Genet 1996; 59 (02) 423-430
  • 34 Rothstein R, Michel B, Gangloff S. Replication fork pausing and recombination or “gimme a break”. Genes Dev 2000; 14 (01) 1-10 Review
  • 35 Watanabe G, Shimizu K. DNA sequence analysis of long PCR amplified products at the D1S80 locus. Leg Med (Tokyo) 2002; 4 (01) 37-39
  • 36 Cohen SM, Furey TS, Doggett NA, Kaufman DG. Genome-wide sequence and functional analysis of early replicating DNA in normal human fibroblasts. BMC Genomics 2006; 7: 301
  • 37 Ekholm-Reed S, Spruck CH, Sangfelt O. et al. Mutation of hCDC4 leads to cell cycle deregulation of cyclin E in cancer. Cancer Res 2004; 64 (03) 795-800
  • 38 Reish O, Orlovski A, Mashevitz M. et al. Modified allelic replication in lymphocytes of patients with neurofibromatosis type 1. Cancer Genet Cytogenet 2003; 143 (02) 133-139
  • 39 Ferreira BI, Alonso J, Carrillo J. et al. Array CGH and gene-expression profiling reveals distinct genomic instability patterns associated with DNA repair and cell-cycle checkpoint pathways in Ewing's sarcoma. Oncogene 2008; 27 (14) 2084-2090
  • 40 Yeshaya J, Shalgi R, Shohat M, Avivi L. FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes. Hum Genet 1999; 105 (1-2): 86-97
  • 41 Nagler A, Cytron S, Mashevich M, Korenstein-Ilan A, Avivi L. The aberrant asynchronous replication—characterizing lymphocytes of cancer patients—is erased following stem cell transplantation. BMC Cancer 2010; 10: 230
  • 42 Hamdan SM, van Oijen AM. Timing, coordination, and rhythm: acrobatics at the DNA replication fork. J Biol Chem 2010; 285 (25) 18979-18983
  • 43 Shetty D, Jain H, Rohil Y. et al. Role of cytogenetic abnormalities detected by fluorescence in situ hybridization as a prognostic marker: pathogenesis & clinical course in patients with B-chronic lymphocytic leukaemia. Indian J Med Res 2021; 153 (04) 475-483