Journal of Molecular Oncology Research

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
Reach Us +1 (202) 780-3397

Short Communication - Journal of Molecular Oncology Research (2022) Volume 6, Issue 2

Misusing autophagy-regulative nanomaterials for actuation of dendritic cells empowers fortified cancer immunotherapy

Behzad Baradn*


Department of Immunology Research Center, University of Medical Sciences, Tabriz, Iran

Corresponding Author:
Behzad Baradn
Department of Immunology Research Center
University of Medical Sciences, Tabriz, Iran

Received: 28-Jan-2022, Manuscript No. AAMOR-22-110; Editor assigned: 31-Jan-2022, Pre QC No. AAMOR-22-110 (PQ); Reviewed: 14-Feb-2022, QC No. AAMOR-22-110; Revised: 19-Feb-2022; AAMOR-22-110 (R); Published: 28-Feb-2022, DOI: 10.35841/aamor-6.2.110

Citation: Baradn B. Misusing autophagy-regulative nanomaterials for actuation of dendritic cells empowers fortified cancer immunotherapy. J Mol Oncol Res. 2022;6(2):110

Visit for more related articles at Journal of Molecular Oncology Research


Dendritic cells (DCs), as the foremost capable antigen displaying cells, play a basic part in directing safe reaction and anti-tumor prepare. In any case, the immunosuppressive cells and variables dwelled within the tumor microenvironment (TME) posture different challenges that can demolish competent DC work comprising antigen introduction and resistant start. In this setting, creating powerful procedures to progress the work of DCs is basically required for progressing the viability of tumor immunotherapy. Autophagy is found to be closely related to the different capacities of DCs beneath physiological and neurotic conditions. Particularly, nanomaterials (NMs) can lock in within the clutter and consistency of autophagy to tweak their digestion system and work of DCs. Sensible plan of nanomaterials with autophagy control is of extraordinary importance to enact DCs and upgrade its immunological capacities, inciting vigorous and strong antitumor insusceptibility. In this survey, we think about the plan and optimization of nanomaterials with the work of controlling DCs autophagy, examine the most component of DCs autophagy initiated by nanomaterials and its application in tumor immunotherapy, advancing the advance and improvement of cancer immunotherapy procedures within the future.


lysosomal action, Antibodies, Immunotherapy.


Dendritic cells are central controllers for the start and upkeep of versatile resistant reaction, preparing powerful effector reactions within the T-cell-mediated cancer immunotherapy [1]. In spite of the predominant potential of DCs to actuate vigorous and strong antitumoral reactions, the immunosuppressive tumor microenvironment can create different components to effectively smother competent DC capacities, particularly DC enactment, coming about in avoiding safe control and as such decreased capacity against cancer [2]. It is basically required for restorative focusing on of DCs to alter DCs from a juvenile tolerogenic state to a develop immunostimulatory phenotype, evoking an viable antitumor resistant reaction [3]. An assortment of state-of- the-art techniques that look for to make strides DC work have developed, such as receptive cell exchange , safe checkpoint barricade , antibodies stacked with antigens and adjuvants , and autophagy direction. Autophagy and resistant direction have the same or related signaling pathways in arrange to be auto-protective for the life form. Numerous ponders have emphasized the balance of DC capacities by autophagy, particularly antigen take-up and introduction require tall levels of endocytic and lysosomal action that are firmly related to autophagy. Nanomaterials characterized fundamentally as great biocompatibility and numerous alteration locales have been illustrated to initiate autophagy irritation in DCs, which can be misused as restorative specialists against tumor. The nanomaterials-induced autophagy is controlled by numerous natural variables extending from destabilization of autophagy- associated particles to stretch reactions of organelles enveloping endoplasmic reticulum push (ERS), mitochondrial harm , and lysosomal brokenness. The unmistakable capacity of nanomaterials depends on its particular harmful impacts through interferometer with atomic pathway after entering the body. Nanomaterial-mediated autophagy can serve a double part in tumor treatment. Beneath different physiological conditions, the level of autophagy required to start a strong anti-tumor resistant reaction is particular or indeed inverse.

The component and effectiveness of cytotoxicity are closely connected with the physical and chemical properties of nanomaterials such as estimate, shape, fabric and surface alteration. Given the chance of their characteristic poisonous quality in DCs, centering on the properties of the nanomaterials is fundamental for balancing the autophagy handle when planning functionalized nanomaterial’s as a viable restorative specialist. The treatment methodology misusing nanomaterial’s to tweak DCs autophagy has shown incredible potential within the treatment of tumor. Autophagy not as it were influences the relocation and development of DCs, but moreover facilitates antigen take-up and introduction, meddling with cytokine emission, and intercedes T cell enactment and separation. Based on these organic capacities, well-designed nanomaterials can take an interest in different levels of DCs resistant work control, particularly in versatile resistant reactions, applying tumor-specific cytotoxic T lymphocyte (CTL) safe impacts. Nanomaterials are at slightest one-dimensional nano-scale materials in three-dimensional space scale, among which nanoparticles (NPs) allude to the particulate nanomaterials. Nanomaterials with a structure measure of 1–100 nm and uncommon physicochemical properties, such as volume impact, surface impact, quantum measure impact, catalytic execution and optical properties, have been broadly utilized within the biomedical field. The enacted DCs have the work of proficient antigen introduction and discharge of resistant invigorating cytokines, which is the preface to realize productive tumor immunotherapy.

Nanomaterials may advance the foundation of DC capacities, counting development, antigen preparing and introduction, and T cell separation in tumor immunotherapy. The phenotypes and digestion system of DCs control the heading and degree of downstream safe reaction against cancer cells. A develop immunostimulatory phenotype tends to encourage the restraint of tumor, whereas a tolerogenic phenotype can advance Treg era and initiate the immunosuppression [4]. The changes of phenotype are subordinate on metabolic control of DCs caused by an assortment of go betweens within the TME, such as vascular endothelial development figure. Investigating the interaction between DCs actuation and cancer-immunity discourse from numerous viewpoints is vital for the improvement of novel anticancer medicate. DCs as the foremost basic connect in invigorating anti-tumor resistant reaction, its actuation and phenotype play a unequivocal part within the heading of ensuing safe reaction and the impact of tumor treatment [5].


  1. Chavez-Dominguez R, Perez-Medina M, Lopez-Gonzalez JS, et al. The double-edge sword of autophagy in cancer: from tumor suppression to pro-tumor activity. Front Oncol. 2020;10:1-19
  2. Indexed at, Google Scholar, Cross Ref

  3. Mulcahy Levy JM, Thorburn A. Autophagy in cancer: Moving from understanding mechanism to improving therapy responses in patients. Cell Death Differ. 2020;27: 843-57
  4. Indexed at, Google Scholar, Cross Ref

  5. Marinkovic M, ?prung M, Buljuba?ic M, et al. Autophagy modulation in cancer: Current knowledge on action and therapy. Oxid Med Cell Longev. 2018.
  6. Indexed at, Google Scholar, Cross Ref

  7. Qu X, Yu J, Bhagat G, et al. Promotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene. J Clin Investig. 2003;112:1809-20
  8. Indexed at, Google Scholar, Cross Ref

  9. Yue Z, Jin S, Yang C, et al. Beclin 1, an autophagy gene essential for early embryonic development, is a haploinsufficient tumor suppressor. Natl Acad Sci. 2003;100:15077-82
  10. Indexed at, Google Scholar, Cross Ref

Get the App