|
1
|
Dohner H: Implication of the molecular
characterization of acute myeloid leukemia. Hematology Am Soc
Hematol Educ Program. 412–419. 2007.PubMed/NCBI
|
|
2
|
Abdel-Wahab O and Levine RL: Mutations in
epigenetic modifiers in the pathogenesis and therapy of acute
myeloid leukemia. Blood. 121:3563–3572. 2013. View Article : Google Scholar : PubMed/NCBI
|
|
3
|
Ghanem H, Tank N and Tabbara IA:
Prognostic implications of genetic aberrations in acute myelogenous
leukemia with normal cytogenetics. Am J Hematol. 87:69–77. 2012.
View Article : Google Scholar : PubMed/NCBI
|
|
4
|
Im AP, Sehgal AR, Carroll MP, Smith BD,
Tefferi A, Johnson DE and Boyiadzis M: DNMT3A and IDH mutations in
acute myeloid leukemia and other myeloid malignancies: Associations
with prognosis and potential treatment strategies. Leukemia.
28:1774–1783. 2014. View Article : Google Scholar : PubMed/NCBI
|
|
5
|
Komanduri KV and Levine RL: Diagnosis and
Therapy of Acute Myeloid Leukemia in the Era of molecular risk
stratification. Annu Rev Med. 67:59–72. 2016. View Article : Google Scholar : PubMed/NCBI
|
|
6
|
Warburg O: On respiratory impairment in
cancer cells. Science. 124:269–270. 1956.PubMed/NCBI
|
|
7
|
Anderson S, Bankier AT, Barrell BG, de
Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA,
Sanger F, et al: Sequence and organization of the human
mitochondrial genome. Nature. 290:457–465. 1981. View Article : Google Scholar : PubMed/NCBI
|
|
8
|
Shoffner JM and Wallace DC: Mitochondrial
genetics: Principles and practice. Am J Hum Genet. 51:1179–1186.
1992.PubMed/NCBI
|
|
9
|
Bianchi NO, Bianchi MS and Richard SM:
Mitochondrial genome instability in human cancers. Mutat Res.
488:9–23. 2001. View Article : Google Scholar : PubMed/NCBI
|
|
10
|
Bendall KE, Macaulay VA, Baker JR and
Sykes BC: Heteroplasmic point mutations in the human mtDNA control
region. Am J Hum Genet. 59:1276–1287. 1996.PubMed/NCBI
|
|
11
|
Lee SR and Han J: Mitochondrial Nucleoid:
Shield and Switch of the Mitochondrial Genome. Oxid Med Cell
Longev. 2017:80609492017. View Article : Google Scholar : PubMed/NCBI
|
|
12
|
Ishikawa K, Takenaga K, Akimoto M,
Koshikawa N, Yamaguchi A, Imanishi H, Nakada K, Honma Y and Hayashi
J: ROS-generating mitochondrial DNA mutations can regulate tumor
cell metastasis. Science. 320:661–664. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
13
|
Lu J, Sharma LK and Bai Y: Implications of
mitochondrial DNA mutations and mitochondrial dysfunction in
tumorigenesis. Cell Res. 19:802–815. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
14
|
Sultana GN, Rahman A, Shahinuzzaman AD,
Begum RA and Hossain CF: Mitochondrial DNA mutations-candidate
biomarkers for breast cancer diagnosis in Bangladesh. Chin J
Cancer. 31:449–454. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
15
|
Kabekkodu SP, Bhat S, Mascarenhas R,
Mallya S, Bhat M, Pandey D, Kushtagi P, Thangaraj K, Gopinath PM
and Satyamoorthy K: Mitochondrial DNA variation analysis in
cervical cancer. Mitochondrion. 16:73–82. 2014. View Article : Google Scholar : PubMed/NCBI
|
|
16
|
Carew JS, Zhou Y, Albitar M, Carew JD,
Keating MJ and Huang P: Mitochondrial DNA mutations in primary
leukemia cells after chemotherapy: Clinical significance and
therapeutic implications. Leukemia. 17:1437–1447. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
17
|
Kwok CS, Quah TC, Ariffin H, Tay SK and
Yeoh AE: Mitochondrial D-loop polymorphisms and mitochondrial DNA
content in childhood acute lymphoblastic leukemia. J Pediatr
Hematol Oncol. 33:e239–e244. 2011. View Article : Google Scholar : PubMed/NCBI
|
|
18
|
Yacoub HA, Mahmoud WM, El-Baz HA, Eid OM,
ELfayoumi RI, Elhamidy SM and Mahmoud MM: Novel mutations in the
displacement loop of mitochondrial DNA are associated with acute
lymphoblastic leukemia: A genetic sequencing study. Asian Pac J
Cancer Prev. 15:9283–9289. 2014. View Article : Google Scholar : PubMed/NCBI
|
|
19
|
Grist SA, Lu XJ and Morley AA:
Mitochondrial mutations in acute leukaemia. Leukemia. 18:1313–1316.
2004. View Article : Google Scholar : PubMed/NCBI
|
|
20
|
Sharawat SK, Bakhshi R, Vishnubhatla S and
Bakhshi S: Mitochondrial D-loop variations in paediatric acute
myeloid leukaemia: A potential prognostic marker. Br J Haematol.
149:391–398. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
21
|
Silkjaer T, Nørgaard JM, Aggerholm A,
Ebbesen LH, Kjeldsen E, Hokland P and Nyvold CG: Characterization
and prognostic significance of mitochondrial DNA variations in
acute myeloid leukemia. Eur J Haematol. 90:385–396. 2013.
View Article : Google Scholar : PubMed/NCBI
|
|
22
|
Sabattini E, Bacci F, Sagramoso C and
Pileri SA: WHO classification of tumours of haematopoietic and
lymphoid tissues in 2008: An overview. Pathologica. 102:83–87.
2010.PubMed/NCBI
|
|
23
|
Xun J, Li Z, Song X and Wang X:
Identification of sequence polymorphisms in the D-loop region of
mitochondrial DNA as risk biomarkers for malignant fibrous
histiocytoma. Mitochondrial DNA. 26:380–383. 2015. View Article : Google Scholar : PubMed/NCBI
|
|
24
|
Nishimaki Y, Sato K, Fang L, Ma M,
Hasekura H and Boettcher B: Sequence polymorphism in the mtDNA HV1
region in Japanese and Chinese. Leg Med (Tokyo). 1:238–249. 1999.
View Article : Google Scholar : PubMed/NCBI
|
|
25
|
Mueller EE, Eder W, Ebner S, Schwaiger E,
Santic D, Kreindl T, Stanger O, Paulweber B, Iglseder B, Oberkofler
H, et al: The mitochondrial T16189C polymorphism is associated with
coronary artery disease in Middle European populations. PLoS One.
6:e164552011. View Article : Google Scholar : PubMed/NCBI
|
|
26
|
Bandelt HJ, Kloss-Brandstätter A, Richards
MB, Yao YG and Logan I: The case for the continuing use of the
revised Cambridge Reference Sequence (rCRS) and the standardization
of notation in human mitochondrial DNA studies. J Hum Genet.
59:66–77. 2014. View Article : Google Scholar : PubMed/NCBI
|
|
27
|
Lee H, Geng C, Cheng M, Lee Z and Guo Z:
Single nucleotide polymorphisms in the mitochondrial displacement
loop and age-at-onset of familial breast cancer. Mitochondrial DNA
A DNA Mapp Seq Anal. 27:3082–3085. 2016.PubMed/NCBI
|
|
28
|
Li S, Wan P, Peng T, Xiao K, Su M, Shang
L, Xu B, Su Z, Ye X and Peng N: Associations between sequence
variations in the mitochondrial DNA D-loop region and outcome of
hepatocellular carcinoma. Oncol Lett. 11:3723–3728. 2016.PubMed/NCBI
|
|
29
|
Wang CY, Li H, Hao XD, Liu J, Wang JX,
Wang WZ, Kong QP and Zhang YP: Uncovering the profile of somatic
mtDNA mutations in Chinese colorectal cancer patients. PLoS One.
6:e216132011. View Article : Google Scholar : PubMed/NCBI
|
|
30
|
Hu WX, Ding CM, Li RJ, Fan HY, Guo ZJ and
Liu W: Single nucleotide polymorphisms in the mitochondrial
displacement loop and age-at-onset of non-small cell lung cancer.
Genet Mol Res. 14:2512–2517. 2015. View Article : Google Scholar : PubMed/NCBI
|
|
31
|
Feng D, Xu H, Li X, Wei Y, Jiang H, Xu H,
Luo A and Zhou F: An association analysis between mitochondrial DNA
content, G10398A polymorphism, HPV infection, and the prognosis of
cervical cancer in the Chinese Han population. Tumour Biol.
37:5599–6007. 2016. View Article : Google Scholar : PubMed/NCBI
|
|
32
|
Lam ET, Bracci PM, Holly EA, Chu C, Poon
A, Wan E, White K, Kwok PY, Pawlikowska L and Tranah GJ:
Mitochondrial DNA sequence variation and risk of pancreatic cancer.
Cancer Res. 72:686–695. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
33
|
Zhang J, Asin-Cayuela J, Fish J, Michikawa
Y, Bonafe M, Olivieri F, Passarino G, De Benedictis G, Franceschi C
and Attardi G: Strikingly higher frequency in centenarians and
twins of mtDNA mutation causing remodeling of replication origin in
leukocytes. Proc Natl Acad Sci USA. 100:1116–1121. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
34
|
Wang Y, Michikawa Y, Mallidis C, Bai Y,
Woodhouse L, Yarasheski KE, Miller CA, Askanas V, Engel WK, Bhasin
S and Attardi G: Muscle-specific mutations accumulate with aging in
critical human mtDNA control sites for replication. Proc Natl Acad
Sci USA. 98:4022–4027. 2001. View Article : Google Scholar : PubMed/NCBI
|
|
35
|
Lee JH, Hwang I, Kang YN, Choi IJ and Kim
DK: Genetic characteristics of mitochondrial DNA was associated
with colorectal carcinogenesis and its prognosis. PLoS One.
10:e01186122015. View Article : Google Scholar : PubMed/NCBI
|
|
36
|
Lee DH, Lee JH, Kim DK and Keum DY:
Nuclear and mitochondrial DNAs microsatellite instability and
mitochondrial DNA copy number in adenocarcinoma and squamous cell
carcinoma of lung: A pilot study. APMIS. 123:1048–1054. 2015.
View Article : Google Scholar : PubMed/NCBI
|
|
37
|
Chen XZ, Fang Y, Shi YH, Cui JH, Li LY, Xu
YC and Ling B: Mitochondrial D310 instability in Chinese lung
cancer patients. Mitochondrial DNA A DNA Mapp Seq Anal.
27:1177–1180. 2016. View Article : Google Scholar : PubMed/NCBI
|
|
38
|
Geurts-Giele WR, Gathier GH, Atmodimedjo
PN, Dubbink HJ and Dinjens WN: Mitochondrial D310 mutation as
clonal marker for solid tumors. Virchows Arch. 467:595–602. 2015.
View Article : Google Scholar : PubMed/NCBI
|
|
39
|
Tipirisetti NR, Govatati S, Pullari P,
Malempati S, Thupurani MK, Perugu S, Guruvaiah P, Rao KL, Digumarti
RR, Nallanchakravarthula V, et al: Mitochondrial control region
alterations and breast cancer risk: A study in South Indian
population. PLoS One. 9:e853632014. View Article : Google Scholar : PubMed/NCBI
|
|
40
|
Wang Y, Liu VW, Tsang PC, Chiu PM, Cheung
AN, Khoo US, Nagley P and Ngan HY: Microsatellite instability in
mitochondrial genome of common female cancers. Int J Gynecol
Cancer. 16 Suppl 1:S259–S266. 2006. View Article : Google Scholar
|
|
41
|
Ye C, Gao YT, Wen W, Breyer JP, Shu XO,
Smith JR, Zheng W and Cai Q: Association of mitochondrial DNA
displacement loop (CA)n dinucleotide repeat polymorphism with
breast cancer risk and survival among Chinese women. Cancer
Epidemiol Biomarkers Prev. 17:2117–2122. 2008. View Article : Google Scholar : PubMed/NCBI
|
