Skip to main content
Log in

Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies

  • Research Article
  • Published:
Frontiers of Medicine Aims and scope Submit manuscript

Abstract

Whether Fanconi anemia (FA) heterozygotes are predisposed to bone marrow failure and hematologic neoplasm is a crucial but unsettled issue in cancer prevention and family consulting. We retrospectively analyzed rare possibly significant variations (PSVs) in the five most obligated FA genes, BRCA2, FANCA, FANCC, FANCD2, and FANCG, in 788 patients with aplastic anemia (AA) and hematologic malignancy. Sixty-eight variants were identified in 66 patients (8.38%). FANCA was the most frequently mutated gene (n = 29), followed by BRCA2 (n = 20). Compared with that of the ExAC East Asian dataset, the overall frequency of rare PSVs was higher in our cohort (P = 0.016). BRCA2 PSVs showed higher frequency in acute lymphocytic leukemia (P = 0.038), and FANCA PSVs were significantly enriched in AA and AML subgroups (P = 0.020; P = 0.008). FA-PSV-positive MDS/AML patients had a higher tumor mutation burden, higher rate of cytogenetic abnormalities, less epigenetic regulation, and fewer spliceosome gene mutations than those of FA-PSV-negative MDS/AML patients (P = 0.024, P = 0.029, P = 0.024, and P = 0.013). The overall PSV enrichment in our cohort suggests that heterozygous mutations of FA genes contribute to hematopoietic failure and leukemogenesis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Swift M. Fanconi’s anaemia in the genetics of neoplasia. Nature 1971; 230(5293): 370–373

    Article  CAS  Google Scholar 

  2. Swerdloow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Arber DA, Hasserjian RP, Le Beau MM, Orazi A, Siebert R. WHO classification of tumours of haematopoietic and lyphoid tissues. 4th ed. International Agency for Research on Cancer, 2017

  3. Rahman N. Realizing the promise of cancer predisposition genes. Nature 2014; 505(7483): 302–308

    Article  CAS  Google Scholar 

  4. Daly MB, Pilarski R, Yurgelun MB, Berry MP, Buys SS, Dickson P, Domchek SM, Elkhanany A, Friedman S, Garber JE, Goggins M, Hutton ML, Khan S, Klein C, Kohlmann W, Kurian AW, Laronga C, Litton JK, Mak JS, Menendez CS, Merajver SD, Norquist BS, Offit K, Pal T, Pederson HJ, Reiser G, Shannon KM, Visvanathan K, Weitzel JN, Wick MJ, Wisinski KB, Dwyer MA, Darlow SD. NCCN guidelines insights: genetic/familial high-risk assessment: breast, ovarian, and pancreatic, Version 1.2020. J Natl Compr Canc Netw 2020; 18(4): 380–391

    Article  Google Scholar 

  5. Mathew CG. Fanconi anaemia genes and susceptibility to cancer. Oncogene 2006; 25(43): 5875–5884

    Article  CAS  Google Scholar 

  6. Berwick M, Satagopan JM, Ben-Porat L, Carlson A, Mah K, Henry R, Diotti R, Milton K, Pujara K, Landers T, Dev Batish S, Morales J, Schindler D, Hanenberg H, Hromas R, Levran O, Auerbach AD. Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancer. Cancer Res 2007; 67(19): 9591–9596

    Article  CAS  Google Scholar 

  7. Tischkowitz M, Easton DF, Ball J, Hodgson SV, Mathew CG. Cancer incidence in relatives of British Fanconi anaemia patients. BMC Cancer 2008; 8(1): 257

    Article  Google Scholar 

  8. Przychodzen B, Makishima H, Sekeres MA, Balasubramanian SK, Thota S, Patel BJ, Clemente M, Hirsch C, Dienes B, Maciejewski JP. Fanconi anemia germline variants as susceptibility factors in aplastic anemia, MDS and AML. Oncotarget 2017; 9(2): 2050–2057

    Article  Google Scholar 

  9. Maung KZY, Leo PJ, Bassal M, Casolari DA, Gray JX, Bray SC, Pederson S, Singhal D, Samaraweera SE, Nguyen T, Cildir G, Marshall M, Ewing A, Duncan EL, Brown MA, Saal R, Tergaonkar V, To LB, Marlton P, Gill D, Lewis I, Deans AJ, Brown AL, D’Andrea RJ, Gonda TJ. Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia. Blood Cancer J 2018; 8(6): 50

    Article  Google Scholar 

  10. Nie D, Cao P, Wang F, Zhang J, Liu M, Zhang W, Liu L, Zhao H, Teng W, Tian W, Chen X, Zhang Y, Nan H, Wei Z, Wang T, Liu H. Analysis of overlapping heterozygous novel submicroscopic CNVs and FANCA-VPS9D1 fusion transcripts in a Fanconi anemia patient. J Hum Genet 2019; 64(9): 899–909

    Article  CAS  Google Scholar 

  11. Zhang Y, Wang F, Chen X, Zhang Y, Wang M, Liu H, Cao P, Ma X, Wang T, Zhang J, Zhang X, Lu P, Liu H. CSF3R mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia. Cancer 2018; 124(16): 3329–3338

    Article  CAS  Google Scholar 

  12. Potter NU, Sarmousakis C, Li FP. Cancer in relatives of patients with aplastic anemia. Cancer Genet Cytogenet 1983; 9(1): 61–65

    Article  CAS  Google Scholar 

  13. Swift M, Caldwell RJ, Chase C. Reassessment of cancer predisposition of Fanconi anemia heterozygotes. J Natl Cancer Inst 1980; 65(5): 863–867

    CAS  PubMed  Google Scholar 

  14. Kutler DI, Singh B, Satagopan J, Batish SD, Berwick M, Giampietro PF, Hanenberg H, Auerbach AD. A 20-year perspective on the International Fanconi Anemia Registry (IFAR). Blood 2003; 101(4): 1249–1256

    Article  CAS  Google Scholar 

  15. Castella M, Pujol R, Callén E, Ramírez MJ, Casado JA, Talavera M, Ferro T, Muñoz A, Sevilla J, Madero L, Cela E, Beléndez C, de Heredia CD, Olivé T, de Toledo JS, Badell I, Estella J, Dasí Á, Rodríguez-Villa A, Gómez P, Tapia M, Molinés A, Figuera Á, Bueren JA, Surrallés J. Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact. J Med Genet 2011; 48(4): 242–250

    Article  Google Scholar 

  16. Flynn EK, Kamat A, Lach FP, Donovan FX, Kimble DC, Narisu N, Sanborn E, Boulad F, Davies SM, Gillio AP3rd, Harris RE, MacMillan ML, Wagner JE Jr, Smogorzewska A, Auerbach AD, Ostrander EA, Chandrasekharappa SC. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes. Hum Mutat 2014; 35(11): 1342–1353

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

This work was partially supported by a grant from the Shandong Nature Science Fund (No. ZR2016HP02).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hongxing Liu.

Additional information

Compliance with ethics guidelines

Daijing Nie, Jing Zhang, Fang Wang, Xvxin Li, Lili Liu, Wei Zhang, Panxiang Cao, Xue Chen, Yang Zhang, Jiaqi Chen, Xiaoli Ma, Xiaosu Zhou, Qisheng Wu, Ming Liu, Mingyue Liu, Wenjun Tian, and Hongxing Liu have no conflict of interest to declare. All procedures followed were in accordance with the ethical standards of the Ethical Committee of Hebei Yanda Lu Daopei Hospital on human experimentation and with the Helsinki Declaration of 1975, as revised in 2000. Informed consent was obtained from all patients for participation in the study.

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nie, D., Zhang, J., Wang, F. et al. Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies. Front. Med. 16, 459–466 (2022). https://doi.org/10.1007/s11684-021-0841-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11684-021-0841-x

Keywords

Navigation