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Article Open Access

BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma

  • Authors:
    • Pei Wan
    • Zhilin Chen
    • Weifeng Zhong
    • Huiming Jiang
    • Zhicheng Huang
    • Dong Peng
    • Qiang He
    • Nanhui Chen
  • View Affiliations / Copyright

    Affiliations: Meizhou People's Hospital (Huangtang Hospital), Meizhou, Guangdong 514031, P.R. China
    Copyright: © Wan et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2475-2486
    |
    Published online on: October 8, 2020
       https://doi.org/10.3892/or.2020.7796
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Abstract

Among all types of kidney diseases, renal cell carcinoma (RCC) has the highest mortality, recurrence and metastasis rates, which results in high numbers of tumor‑associated mortalities in China. Identifying a novel therapeutic target has attracted increasing attention. Bromodomain and extraterminal domain (BET) proteins have the ability to read the epigenome, leading to regulation of gene transcription. As an important member of the BET family, bromodomain testis‑specific protein (BRDT) has been well studied; however, the mechanism underlying BRDT in the regulation of RCC has not been fully investigated. Eukaryotic translation initiation factor 4E‑binding protein 1 (eIF4EBP1) is a binding partner of eIF4E that is involved in affecting the progression of various cancer types via regulating gene transcription. To identify novel regulators of eIF4EBP1, an immunoprecipitation assay and mass spectrometry analysis was performed in RCC cells. It was revealed that eIF4EBP1 interacted with BRDT, a novel interacting protein. In addition, the present study further demonstrated that BRDT inhibitors PLX51107 and INCB054329 blocked the progression of RCC cells, along with suppressing eIF4EBP1 and c‑myc expression. Small interfering (si) RNAs were used to knock down BRDT expression, which suppressed RCC cell proliferation and eIF4EBP1 protein expression. In addition, overexpression of eIF4EBP1 partially abolished the inhibited growth function of PLX51107 but knocking down eIF4EBP1 improved the inhibitory effects of PLX51107. Furthermore, treatment with PLX51107 or knockdown of BRDT expression decreased c‑myc expression at both the mRNA and protein levels, and attenuated its promoter activity, as determined by luciferase reporter assays. PLX51107 also significantly altered the interaction between the c‑myc promoter with eIF4EBP1 and significantly attenuated the increase of RCC tumors, accompanied by decreased c‑myc mRNA and protein levels in vivo. Taken together, these data suggested that blocking of BRDT by PLX51107, INCB054329 or BRDT knockdown suppressed the growth of RCC via decreasing eIF4EBP1, thereby leading to decreased c‑myc transcription levels. Considering the regulatory function of BET proteins in gene transcription, the present study suggested that there is a novel mechanism underlying eIF4EBP1 regulation by BRDT, and subsequently decreased c‑myc in RCC, and further identified a new approach by regulating eIF4EBP1 or c‑myc for enhancing BRDT‑targeting RCC therapy.
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1 

Cella D, Grünwald V, Escudier B, Hammers HJ, George S, Nathan P, Grimm MO, Rini BI, Doan J, Ivanescu C, et al: Patient-Reported outcomes of patients with advanced renal cell carcinoma treated with nivolumab plus ipilimumab versus sunitinib (CheckMate 214): A randomised, phase 3 trial. Lancet Oncol. 20:297–310. 2019. View Article : Google Scholar : PubMed/NCBI

2 

Powles T: Re: Nivolumab plus ipilimumab versus sunitinib in advanced renal-cell carcinoma. Eur Urol. 74:679–680. 2018. View Article : Google Scholar : PubMed/NCBI

3 

Chevrier S, Levine JH, Zanotelli VR, Silina K, Schulz D, Bacac M, Ries CH, Ailles L, Jewett MA, Moch H, et al: An immune atlas of clear cell renal cell carcinoma. Cell. 169:736–749. 2017. View Article : Google Scholar : PubMed/NCBI

4 

Song E, Song W, Ren M, Xing L, Ni W, Li Y, Gong M, Zhao M, Ma X, Zhang X and An R: Identification of potential crucial genes associated with carcinogenesis of clear cell renal cell carcinoma. J Cell Biochem. 119:5163–5174. 2018. View Article : Google Scholar : PubMed/NCBI

5 

Wang Q, Ding H, He Y, Li X, Cheng Y, Xu Q, Yang Y, Liao G, Meng X, Huang C and Li J: NLRC5 mediates cell proliferation, migration, and invasion by regulating the wnt/β-catenin signalling pathway in clear cell renal cell carcinoma. Cancer Lett. 444:9–19. 2019. View Article : Google Scholar : PubMed/NCBI

6 

Zhang X, Yan L, Jiao W, Ren J, Xing N, Zhang Y, Zang Y, Wang J and Xu Z: The clinical and biological significance of MICA in clear cell renal cell carcinoma patients. Tumour Biol. 37:2153–2159. 2016. View Article : Google Scholar : PubMed/NCBI

7 

Zhu H, Wang Z, Xu Q, Zhang Y, Zhai Y, Bai J, Liu M, Hui Z and Xu N: Inhibition of STAT1 sensitizes renal cell carcinoma cells to radiotherapy and chemotherapy. Cancer Biol Ther. 13:401–407. 2012. View Article : Google Scholar : PubMed/NCBI

8 

Wozniak MB, Le Calvez-Kelm F, Abedi-Ardekani B, Byrnes G, Durand G, Carreira C, Michelon J, Janout V, Holcatova I, Foretova L, et al: Integrative genome-wide gene expression profiling of clear cell renal cell carcinoma in czech republic and in the United States. PLoS One. 8:e578862013. View Article : Google Scholar : PubMed/NCBI

9 

Wu J, Wang H, Ricketts CJ, Yang Y, Merino MJ, Zhang H, Shi G, Gan H, Linehan WM, Zhu Y and Ye D: Germline mutations of renal cancer predisposition genes and clinical relevance in Chinese patients with sporadic, early-onset disease. Cancer. 125:1060–1069. 2019. View Article : Google Scholar : PubMed/NCBI

10 

Ghatalia P, Gordetsky J, Kuo F, Dulaimi E, Cai KQ, Devarajan K, Bae S, Naik G, Chan TA, Uzzo R, et al: Prognostic impact of immune gene expression signature and tumor infiltrating immune cells in localized clear cell renal cell carcinoma. J Immunother Cancer. 7:1392019. View Article : Google Scholar : PubMed/NCBI

11 

Pal S, Gong J, Mhatre SK, Lin SW, Surinach A, Ogale S, Vohra R, Wallen H and George D: Real-World treatment patterns and adverse events in metastatic renal cell carcinoma from a large US claims database. BMC Cancer. 19:5482019. View Article : Google Scholar : PubMed/NCBI

12 

Karner C, Kew K, Wakefield V, Masento N and Edwards SJ: Targeted therapies for previously treated advanced or metastatic renal cell carcinoma: Systematic review and network meta-analysis. BMJ Open. 9:e246912019. View Article : Google Scholar

13 

Suarez-Alvarez B, Morgado-Pascual JL, Rayego-Mateos S, Rodriguez RM, Rodrigues-Diez R, Cannata-Ortiz P, Sanz AB, Egido J, Tharaux PL, Ortiz A, et al: Inhibition of bromodomain and extraterminal domain family proteins ameliorates experimental renal damage. J Am Soc Nephrol. 28:504–519. 2017. View Article : Google Scholar : PubMed/NCBI

14 

McDaniel KF, Wang L, Soltwedel T, Fidanze SD, Hasvold LA, Liu D, Mantei RA, Pratt JK, Sheppard GS, Bui MH, et al: Discovery of N-(4-(2,4-Difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)ethanesulfonamide (ABBV-075/Mivebresib), a potent and orally available bromodomain and extraterminal domain (BET) family bromodomain inhibitor. J Med Chem. 60:8369–8384. 2017. View Article : Google Scholar : PubMed/NCBI

15 

Manterola M, Brown TM, Oh MY, Garyn C, Gonzalez BJ and Wolgemuth DJ: BRDT is an essential epigenetic regulator for proper chromatin organization, silencing of sex chromosomes and crossover formation in male meiosis. PLoS Genet. 14:e10072092018. View Article : Google Scholar : PubMed/NCBI

16 

De Rijck J, de Kogel C, Demeulemeester J, Vets S, El Ashkar S, Malani N, Bushman FD, Landuyt B, Husson SJ, Busschots K, et al: The BET family of proteins targets moloney murine leukemia virus integration near transcription start sites. Cell Rep. 5:886–894. 2013. View Article : Google Scholar : PubMed/NCBI

17 

Dibenedetto AJ, Guinto JB, Ebert TD, Bee KJ, Schmidt MM and Jackman TR: Zebrafish brd2a and brd2b are paralogous members of the bromodomain-ET (BET) family of transcriptional coregulators that show structural and expression divergence. BMC Dev Biol. 8:392008. View Article : Google Scholar : PubMed/NCBI

18 

Wang L and Wolgemuth DJ: BET protein BRDT complexes with HDAC1, PRMT5, and TRIM28 and functions in transcriptional repression during spermatogenesis. J Cell Biochem. 117:1429–1438. 2016. View Article : Google Scholar : PubMed/NCBI

19 

Pivot-Pajot C, Caron C, Govin J, Vion A, Rousseaux S and Khochbin S: Acetylation-Dependent chromatin reorganization by BRDT, a testis-specific bromodomain-containing protein. Mol Cell Biol. 23:5354–5365. 2003. View Article : Google Scholar : PubMed/NCBI

20 

Bourova-Flin E, Chuffart F, Rousseaux S and Khochbin S: The role of bromodomain testis-specific factor, BRDT, in cancer: A biomarker and a possible therapeutic target. Cell J. 19:1–8. 2017.PubMed/NCBI

21 

Barda S, Yogev L, Paz G, Yavetz H, Lehavi O, Hauser R, Doniger T, Breitbart H and Kleiman SE: BRDT gene sequence in human testicular pathologies and the implication of its single nucleotide polymorphism (rs3088232) on fertility. Andrology. 2:641–647. 2014. View Article : Google Scholar : PubMed/NCBI

22 

Suyama T, Shiraishi T, Zeng Y, Yu W, Parekh N, Vessella RL, Luo J, Getzenberg RH and Kulkarni P: Expression of cancer/testis antigens in prostate cancer is associated with disease progression. Prostate. 70:1778–1787. 2010. View Article : Google Scholar : PubMed/NCBI

23 

Lagerholm S, Lagerholm S, Dutta S and Nair P: Non-Invasive detection of c-myc p64, c-myc p67 and c-erbb-2 in colorectal cancer. Scand J Gastroenterol. 40:1343–1350. 2005. View Article : Google Scholar : PubMed/NCBI

24 

Ozer HG, El-Gamal D, Powell B, Hing ZA, Blachly JS, Harrington B, Mitchell S, Grieselhuber NR, Williams K, Lai TH, et al: BRD4 profiling identifies critical chronic lymphocytic leukemia oncogenic circuits and reveals sensitivity to PLX51107, a novel structurally distinct BET inhibitor. Cancer Discov. 8:458–477. 2018. View Article : Google Scholar : PubMed/NCBI

25 

Erkes DA, Field CO, Capparelli C, Tiago M, Purwin TJ, Chervoneva I, Berger AC, Hartsough EJ, Villanueva J and Aplin AE: The next-generation BET inhibitor, PLX51107, delays melanoma growth in a CD8-mediated manner. Pigment Cell Melanoma Res. 32:687–696. 2019.PubMed/NCBI

26 

Stubbs MC, Burn TC, Sparks R, Maduskuie T, Diamond S, Rupar M, Wen X, Volgina A, Zolotarjova N, Waeltz P, et al: The novel bromodomain and extraterminal domain inhibitor INCB054329 induces vulnerabilities in myeloma cells that inform rational combination strategies. Clin Cancer Res. 25:300–311. 2019. View Article : Google Scholar : PubMed/NCBI

27 

Wilson AJ, Stubbs M, Liu P, Ruggeri B and Khabele D: The BET inhibitor INCB054329 reduces homologous recombination efficiency and augments PARP inhibitor activity in ovarian cancer. Gynecol Oncol. 149:575–584. 2018. View Article : Google Scholar : PubMed/NCBI

28 

Yao Z, Yang S, Zhao H, Yang H and Jiang X: BET inhibitor I-BET151 sensitizes GBM cells to temozolomide via PUMA induction. Cancer Gene Ther. 27:226–234. 2019. View Article : Google Scholar : PubMed/NCBI

29 

Guo NH, Zheng JF, Zi FM and Cheng J: I-BET151 suppresses osteoclast formation and inflammatory cytokines secretion by targetting BRD4 in multiple myeloma. Biosci Rep. 39:BSR201812452019. View Article : Google Scholar : PubMed/NCBI

30 

Wang C, Cigliano A, Jiang L, Li X, Fan B, Pilo MG, Liu Y, Gui B, Sini M, Smith JW, et al: 4EBP1/eIF4E and p70S6K/RPS6 axes play critical and distinct roles in hepatocarcinogenesis driven by AKT and N-Ras proto-oncogenes in mice. Hepatology. 61:200–213. 2015. View Article : Google Scholar : PubMed/NCBI

31 

Chao MW, Wang LT, Lai CY, Yang XM, Cheng YW, Lee KH, Pan SL and Teng CM: eIF4E binding protein 1 expression is associated with clinical survival outcomes in colorectal cancer. Oncotarget. 6:24092–24104. 2015. View Article : Google Scholar : PubMed/NCBI

32 

William M, Leroux LP, Chaparro V, Lorent J, Graber TE, M'Boutchou MN, Charpentier T, Fabié A, Dozois CM, Stäger S, et al: eIF4E-Binding proteins 1 and 2 limit macrophage anti-inflammatory responses through translational repression of IL-10 and cyclooxygenase-2. J Immunol. 200:4102–4116. 2018. View Article : Google Scholar : PubMed/NCBI

33 

Bao Y, Wu X, Chen J, Hu X, Zeng F, Cheng J, Jin H, Lin X and Chen LF: Brd4 modulates the innate immune response through mnk2-eIF4E pathway-dependent translational control of IkBα. Proc Natl Acad Sci USA. 114:E3993–E4001. 2017. View Article : Google Scholar : PubMed/NCBI

34 

Batool A, Majeed ST, Aashaq S, Majeed R, Shah G, Nazir N and Andrabi KI: Eukaryotic initiation factor 4E (eIF4E) sequestration mediates 4E-BP1 response to rapamycin. Int J Biol Macromol. 125:651–659. 2019. View Article : Google Scholar : PubMed/NCBI

35 

Modrak-Wojcik A, Gorka M, Niedzwiecka K, Zdanowski K, Zuberek J, Niedzwiecka A and Stolarski R: Eukaryotic translation initiation is controlled by cooperativity effects within ternary complexes of 4E-BP1, eIF4E, and the mRNA 5′ cap. FEBS Lett. 587:3928–3934. 2013. View Article : Google Scholar : PubMed/NCBI

36 

Gao W, Lam JW, Li JZ, Chen SQ, Tsang RK, Chan JY and Wong TS: MicroRNA-138-5p controls sensitivity of nasopharyngeal carcinoma to radiation by targeting EIF4EBP1. Oncol Rep. 37:913–920. 2017. View Article : Google Scholar : PubMed/NCBI

37 

Cha YL, Li PD, Yuan LJ, Zhang MY, Zhang YJ, Rao HL, Zhang HZ, Zheng XF and Wang HY: EIF4EBP1 overexpression is associated with poor survival and disease progression in patients with hepatocellular carcinoma. PLoS One. 10:e1174932015. View Article : Google Scholar

38 

Wang Z, Feng X, Molinolo AA, Martin D, Vitale-Cross L, Nohata N, Ando M, Wahba A, Amornphimoltham P, Wu X, et al: 4E-BP1 is a tumor suppressor protein reactivated by mTOR inhibition in head and neck cancer. Cancer Res. 79:1438–1450. 2019. View Article : Google Scholar : PubMed/NCBI

39 

Furic L, Rong L, Larsson O, Koumakpayi IH, Yoshida K, Brueschke A, Petroulakis E, Robichaud N, Pollak M, Gaboury LA, et al: EIF4E phosphorylation promotes tumorigenesis and is associated with prostate cancer progression. Proc Natl Acad Sci USA. 107:14134–14139. 2010. View Article : Google Scholar : PubMed/NCBI

40 

D'Abronzo LS and Ghosh PM: EIF4E phosphorylation in prostate cancer. Neoplasia. 20:563–573. 2018. View Article : Google Scholar : PubMed/NCBI

41 

Lee M, Kim EJ and Jeon MJ: MicroRNAs 125a and 125b inhibit ovarian cancer cells through post-transcriptional inactivation of EIF4EBP1. Oncotarget. 7:8726–8742. 2016. View Article : Google Scholar : PubMed/NCBI

42 

Livak KJ and Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 25:402–408. 2001. View Article : Google Scholar : PubMed/NCBI

43 

Delmore JE, Issa GC, Lemieux ME, Rahl PB, Shi J, Jacobs HM, Kastritis E, Gilpatrick T, Paranal RM, Qi J, et al: BET bromodomain inhibition as a therapeutic strategy to target c-myc. Cell. 146:904–917. 2011. View Article : Google Scholar : PubMed/NCBI

44 

Bandopadhayay P, Bergthold G, Nguyen B, Schubert S, Gholamin S, Tang Y, Bolin S, Schumacher SE, Zeid R, Masoud S, et al: BET bromodomain inhibition of MYC-amplified medulloblastoma. Clin Cancer Res. 20:912–925. 2014. View Article : Google Scholar : PubMed/NCBI

45 

Coudé MM, Braun T, Berrou J, Dupont M, Bertrand S, Masse A, Raffoux E, Itzykson R, Delord M, Riveiro ME, et al: BET inhibitor OTX015 targets BRD2 and BRD4 and decreases c-MYC in acute leukemia cells. Oncotarget. 6:17698–17712. 2015. View Article : Google Scholar : PubMed/NCBI

46 

Baker EK, Taylor S, Gupte A, Sharp PP, Walia M, Walsh NC, Zannettino AC, Chalk AM, Burns CJ and Walkley CR: BET inhibitors induce apoptosis through a MYC independent mechanism and synergise with CDK inhibitors to kill osteosarcoma cells. Sci Rep. 5:101202015. View Article : Google Scholar : PubMed/NCBI

47 

Shao Q, Kannan A, Lin Z, Stack BJ, Suen JY and Gao L: BET protein inhibitor JQ1 attenuates myc-amplified MCC tumor growth in vivo. Cancer Res. 74:7090–7102. 2014. View Article : Google Scholar : PubMed/NCBI

48 

Shi J, Wang Y, Zeng L, Wu Y, Deng J, Zhang Q, Lin Y, Li J, Kang T, Tao M, et al: Disrupting the interaction of BRD4 with diacetylated twist suppresses tumorigenesis in basal-like breast cancer. Cancer Cell. 25:210–225. 2014. View Article : Google Scholar : PubMed/NCBI

49 

Takashima Y, Kikuchi E, Kikuchi J, Suzuki M, Kikuchi H, Maeda M, Shoji T, Furuta M, Kinoshita I, Dosaka-Akita H, et al: Bromodomain and extraterminal domain inhibition synergizes with WEE1-inhibitor AZD1775 effect by impairing non-homologous end joining and enhancing DNA damage in non-small cell lung cancer. Int J Cancer. 15:1114–1124. 2019.

50 

Wang SS, Chen G, Li SH, Pang JS, Cai KT, Yan HB, Huang ZG and He RQ: Identification and validation of an individualized autophagy-clinical prognostic index in bladder cancer patients. Onco Targets Ther. 12:3695–3712. 2019. View Article : Google Scholar : PubMed/NCBI

51 

Wei W, Cao W, Zhan Z, Yan L, Xie Y and Xiao Q: MiR-1284 suppresses gastric cancer progression by targeting EIF4A1. Onco Targets Ther. 12:3965–3976. 2019. View Article : Google Scholar : PubMed/NCBI

52 

Xing ZY, Wang Y, Cheng L, Chen J, He XZ and Xing W: Bromodomain-Containing protein 4 (BRD4) inhibition sensitizes palomid 529-induced anti-renal cell carcinoma cell activity in vitro and in vivo. Cell Physiol Biochem. 50:640–653. 2018. View Article : Google Scholar : PubMed/NCBI

53 

Liao S, Maertens O, Cichowski K and Elledge SJ: Genetic modifiers of the BRD4-NUT dependency of NUT midline carcinoma uncovers a synergism between BETis and CDK4/6is. Genes Dev. 32:1188–1200. 2018. View Article : Google Scholar : PubMed/NCBI

54 

Tan Y, Wang L, Du Y, Liu X, Chen Z, Weng X, Guo J, Chen H, Wang M and Wang X: Inhibition of BRD4 suppresses tumor growth in prostate cancer via the enhancement of FOXO1 expression. Int J Oncol. 53:2503–2517. 2018.PubMed/NCBI

55 

Gao Z, Yuan T, Zhou X, Ni P, Sun G, Li P, Cheng Z and Wang X: Targeting BRD4 proteins suppresses the growth of NSCLC through downregulation of eIF4E expression. Cancer Biol Ther. 19:407–415. 2018. View Article : Google Scholar : PubMed/NCBI

56 

Hsu HS, Lin MH, Jang YH, Kuo TT, Liu CC and Cheng TH: The 4E-BP1/eIF4E ratio is a determinant for rapamycin response in esophageal cancer cells. J Thorac Cardiovasc Surg. 149:378–385. 2015. View Article : Google Scholar : PubMed/NCBI

57 

Wang H, Liu Y, Ding J, Huang Y, Liu J, Liu N, Ao Y, Hong Y, Wang L, Zhang L, et al: Targeting mTOR suppressed colon cancer growth through 4EBP1/eIF4E/PUMA pathway. Cancer Gene Ther. 27:448–460. 2020. View Article : Google Scholar : PubMed/NCBI

58 

Schwartz YB, Kahn TG, Stenberg P, Ohno K, Bourgon R and Pirrotta V: Alternative epigenetic chromatin states of polycomb target genes. PLoS Genet. 6:e10008052010. View Article : Google Scholar : PubMed/NCBI

59 

Thieffry D and Sanchez L: Alternative epigenetic states understood in terms of specific regulatory structures. Ann N Y Acad Sci. 981:135–153. 2002. View Article : Google Scholar : PubMed/NCBI

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Copy and paste a formatted citation
Spandidos Publications style
Wan P, Chen Z, Zhong W, Jiang H, Huang Z, Peng D, He Q and Chen N: BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma. Oncol Rep 44: 2475-2486, 2020.
APA
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D. ... Chen, N. (2020). BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma. Oncology Reports, 44, 2475-2486. https://doi.org/10.3892/or.2020.7796
MLA
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D., He, Q., Chen, N."BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma". Oncology Reports 44.6 (2020): 2475-2486.
Chicago
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D., He, Q., Chen, N."BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma". Oncology Reports 44, no. 6 (2020): 2475-2486. https://doi.org/10.3892/or.2020.7796
Copy and paste a formatted citation
x
Spandidos Publications style
Wan P, Chen Z, Zhong W, Jiang H, Huang Z, Peng D, He Q and Chen N: BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma. Oncol Rep 44: 2475-2486, 2020.
APA
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D. ... Chen, N. (2020). BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma. Oncology Reports, 44, 2475-2486. https://doi.org/10.3892/or.2020.7796
MLA
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D., He, Q., Chen, N."BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma". Oncology Reports 44.6 (2020): 2475-2486.
Chicago
Wan, P., Chen, Z., Zhong, W., Jiang, H., Huang, Z., Peng, D., He, Q., Chen, N."BRDT is a novel regulator of eIF4EBP1 in renal cell carcinoma". Oncology Reports 44, no. 6 (2020): 2475-2486. https://doi.org/10.3892/or.2020.7796
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