State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia

Research output: Contribution to journalReviewResearchpeer-review

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State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia. / Mirzaei, Hamed; Fathullahzadeh, Sima; Khanmohammadi, Razieh; Darijani, Mansoreh; Momeni, Fatemeh; Masoudifar, Aria; Goodarzi, Mohammad; Mardanshah, Omid; Stenvang, Jan; Jaafari, Mahmoud Reza; Mirzaei, Hamid Reza.

In: Journal of Cellular Physiology, Vol. 233, No. 2, 02.2018, p. 888-900.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Mirzaei, H, Fathullahzadeh, S, Khanmohammadi, R, Darijani, M, Momeni, F, Masoudifar, A, Goodarzi, M, Mardanshah, O, Stenvang, J, Jaafari, MR & Mirzaei, HR 2018, 'State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia', Journal of Cellular Physiology, vol. 233, no. 2, pp. 888-900. https://doi.org/10.1002/jcp.25799

APA

Mirzaei, H., Fathullahzadeh, S., Khanmohammadi, R., Darijani, M., Momeni, F., Masoudifar, A., Goodarzi, M., Mardanshah, O., Stenvang, J., Jaafari, M. R., & Mirzaei, H. R. (2018). State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia. Journal of Cellular Physiology, 233(2), 888-900. https://doi.org/10.1002/jcp.25799

Vancouver

Mirzaei H, Fathullahzadeh S, Khanmohammadi R, Darijani M, Momeni F, Masoudifar A et al. State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia. Journal of Cellular Physiology. 2018 Feb;233(2):888-900. https://doi.org/10.1002/jcp.25799

Author

Mirzaei, Hamed ; Fathullahzadeh, Sima ; Khanmohammadi, Razieh ; Darijani, Mansoreh ; Momeni, Fatemeh ; Masoudifar, Aria ; Goodarzi, Mohammad ; Mardanshah, Omid ; Stenvang, Jan ; Jaafari, Mahmoud Reza ; Mirzaei, Hamid Reza. / State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia. In: Journal of Cellular Physiology. 2018 ; Vol. 233, No. 2. pp. 888-900.

Bibtex

@article{0835399b15ec4bc78367170472cfab9e,
title = "State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia",
abstract = "Early diagnostic is one of the most important steps in cancer therapy which helps to design and choose a better therapeutic approach. The finding of biomarkers in various levels including genomics, transcriptomics, and proteomics levels could provide better treatment for various cancers such as chronic lymphocytic leukemia (CLL). The CLL is the one of main lymphoid malignancies which is specified by aggregation of mature B lymphocytes. Among different biomarkers (e.g., CD38, chromosomes abnormalities, ZAP-70, TP53, and microRNA [miRNA]), miRNAs have appeared as new diagnostic and therapeutic biomarkers in patients with the CLL disease. Multiple lines of evidence indicated that deregulation of miRNAs could be associated with pathological events which are present in the CLL. These molecules have an effect on a variety of targets such as Bcl2, c-fos, c-Myc, TP53, TCL1, and STAT3 which play critical roles in the CLL pathogenesis. It has been shown that expression of miRNAs could lead to the activation of B cells and B cell antigen receptor (BCR). Moreover, exosomes containing miRNAs are one of the other molecules which could contribute to BCR stimulation and progression of CLL cells. Hence, miRNAs and exosomes released from CLL cells could be used as potential diagnostic and therapeutic biomarkers for CLL. This critical review focuses on a very important aspect of CLL based on biomarker discovery covers the pros and cons of using miRNAs as important diagnostics and therapeutics biomarkers for this deadly disease.",
keywords = "biomarker, chronic lymphocytic leukemia, diagnosis, MicroRNA, therapy",
author = "Hamed Mirzaei and Sima Fathullahzadeh and Razieh Khanmohammadi and Mansoreh Darijani and Fatemeh Momeni and Aria Masoudifar and Mohammad Goodarzi and Omid Mardanshah and Jan Stenvang and Jaafari, {Mahmoud Reza} and Mirzaei, {Hamid Reza}",
year = "2018",
month = feb,
doi = "10.1002/jcp.25799",
language = "English",
volume = "233",
pages = "888--900",
journal = "Journal of Cellular Physiology",
issn = "0021-9541",
publisher = "JohnWiley & Sons, Inc.",
number = "2",

}

RIS

TY - JOUR

T1 - State of the art in microRNA as diagnostic and therapeutic biomarkers in chronic lymphocytic leukemia

AU - Mirzaei, Hamed

AU - Fathullahzadeh, Sima

AU - Khanmohammadi, Razieh

AU - Darijani, Mansoreh

AU - Momeni, Fatemeh

AU - Masoudifar, Aria

AU - Goodarzi, Mohammad

AU - Mardanshah, Omid

AU - Stenvang, Jan

AU - Jaafari, Mahmoud Reza

AU - Mirzaei, Hamid Reza

PY - 2018/2

Y1 - 2018/2

N2 - Early diagnostic is one of the most important steps in cancer therapy which helps to design and choose a better therapeutic approach. The finding of biomarkers in various levels including genomics, transcriptomics, and proteomics levels could provide better treatment for various cancers such as chronic lymphocytic leukemia (CLL). The CLL is the one of main lymphoid malignancies which is specified by aggregation of mature B lymphocytes. Among different biomarkers (e.g., CD38, chromosomes abnormalities, ZAP-70, TP53, and microRNA [miRNA]), miRNAs have appeared as new diagnostic and therapeutic biomarkers in patients with the CLL disease. Multiple lines of evidence indicated that deregulation of miRNAs could be associated with pathological events which are present in the CLL. These molecules have an effect on a variety of targets such as Bcl2, c-fos, c-Myc, TP53, TCL1, and STAT3 which play critical roles in the CLL pathogenesis. It has been shown that expression of miRNAs could lead to the activation of B cells and B cell antigen receptor (BCR). Moreover, exosomes containing miRNAs are one of the other molecules which could contribute to BCR stimulation and progression of CLL cells. Hence, miRNAs and exosomes released from CLL cells could be used as potential diagnostic and therapeutic biomarkers for CLL. This critical review focuses on a very important aspect of CLL based on biomarker discovery covers the pros and cons of using miRNAs as important diagnostics and therapeutics biomarkers for this deadly disease.

AB - Early diagnostic is one of the most important steps in cancer therapy which helps to design and choose a better therapeutic approach. The finding of biomarkers in various levels including genomics, transcriptomics, and proteomics levels could provide better treatment for various cancers such as chronic lymphocytic leukemia (CLL). The CLL is the one of main lymphoid malignancies which is specified by aggregation of mature B lymphocytes. Among different biomarkers (e.g., CD38, chromosomes abnormalities, ZAP-70, TP53, and microRNA [miRNA]), miRNAs have appeared as new diagnostic and therapeutic biomarkers in patients with the CLL disease. Multiple lines of evidence indicated that deregulation of miRNAs could be associated with pathological events which are present in the CLL. These molecules have an effect on a variety of targets such as Bcl2, c-fos, c-Myc, TP53, TCL1, and STAT3 which play critical roles in the CLL pathogenesis. It has been shown that expression of miRNAs could lead to the activation of B cells and B cell antigen receptor (BCR). Moreover, exosomes containing miRNAs are one of the other molecules which could contribute to BCR stimulation and progression of CLL cells. Hence, miRNAs and exosomes released from CLL cells could be used as potential diagnostic and therapeutic biomarkers for CLL. This critical review focuses on a very important aspect of CLL based on biomarker discovery covers the pros and cons of using miRNAs as important diagnostics and therapeutics biomarkers for this deadly disease.

KW - biomarker

KW - chronic lymphocytic leukemia

KW - diagnosis

KW - MicroRNA

KW - therapy

U2 - 10.1002/jcp.25799

DO - 10.1002/jcp.25799

M3 - Review

C2 - 28084621

AN - SCOPUS:85014805815

VL - 233

SP - 888

EP - 900

JO - Journal of Cellular Physiology

JF - Journal of Cellular Physiology

SN - 0021-9541

IS - 2

ER -

ID: 194913528