4.5 Article

Irradiation of breast cancer cells enhances CXCL16 ligand expression and induces the migration of natural killer cells expressing the CXCR6 receptor

Journal

CYTOTHERAPY
Volume 18, Issue 12, Pages 1532-1542

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jcyt.2016.08.006

Keywords

CXCL16; ionizing radiation; immunotherapy; migration; NK cells

Funding

  1. National Research Foundation of Korea [2013R1A1A 2063510, 2015M2B2A9029388]
  2. Korea Research Institute of Bioscience and Biotechnology [KGM4941511]
  3. Pioneer Research Center Program through National Research Foundation of Korea - Ministry of Science, ICT & Future Planning [2015M3C1A3056410]
  4. National Research Council of Science & Technology (NST), Republic of Korea [KGM4941511] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2015M2B2A9029388] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

Background aims. Few studies have examined the migration pattern of natural killer (NK) cells, especially after radiation treatment for cancer. We investigated whether irradiation can modulate the expression of chemokines in cancer cells and the migration of NK cells to irradiated tumor cells. Methods. The expression of chemokine receptors (CXCR3, CXCR4 and CXCR6) on interleukin-2 (IL-2)/IL-15-activated NK cells was assessed using flow cytometry. Related chemokine ligands (CXCL11, CXCL12 and CXCL16) in human breast cancer cell lines (MCF7, SKBR3 and MDA-MB231) irradiated at various doses were assessed using reverse transcription polymerase chain reaction (RT-PCR), fluorescence-activated cell sorting (FAGS) and enzyme-linked immunosorbent assay (ELISA). The cell-free culture supernatant was collected 96 h after irradiation of breast cancer cell lines for migration and blocking assays. Results. The activated NK cells expressed CXCR6. Expression of the CXCR6 ligand CXCL16 increased in a time- and dose-dependent manner in all analyzed cancer cell lines. CXCL16 expression was statistically significantly enhanced in all breast cancer cell lines on day 3 after 20 Gy irradiation. Activated NK. cells migration correlated with CXCL16 concentration (R-2 = 0.91; P < 0.0001). Significantly enhanced migration of NK cells to irradiated cancer cells was observed for a dose of 20 Gy in MCF7 (P=0.043) and SKBR3 (P=0.043) cells, but not in MDA-MB231 (P=0.225) cells. A blocking assay using a CXCR6 antibody showed a significant decrease in the migration of activated NK cells in all cancer cell lines. Conclusions. Our data indicate that irradiation induces CXCL16 chemokine expression in cancer cells and enhances the migration of activated NK cells expressing CXCR6 to irradiated breast cancer cells. These results suggest that radiation would improve the anti-tumor effect of NK cells through enhanced migration of NK cells to tumor site for the treatment of patients with breast cancer.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Multidisciplinary Sciences

Efficient RNA drug delivery using red blood cell extracellular vesicles

Waqas Muhammad Usman, Tin Chanh Pham, Yuk Yan Kwok, Luyen Tien Vu, Victor Ma, Boya Peng, Yuen San Chan, Likun Wei, Siew Mei Chin, Ajijur Azad, Alex Bai-Liang He, Anskar Y. H. Leung, Mengsu Yang, Ng Shyh-Chang, William C. Cho, Jiahai Shi, Minh T. N. Le

NATURE COMMUNICATIONS (2018)

Article Oncology

Combined NK Cell Therapy and Radiation Therapy Exhibit Long-Term Therapeutic and Antimetastatic Effects in a Human Triple Negative Breast Cancer Model

Kyung Won Kim, Jae-UK Jeong, Kyung-Hwa Lee, Tung Nguyen Thanh Uong, Joon Haeng Rhee, Sung-Ja Ahn, Sang-Ki Kim, Duck Cho, Huy Phuoc Quang Nguyen, Chanh Tin Pham, Mee Sun Yoon

INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS (2020)

Article Oncology

Extracellular vesicles as natural therapeutic agents and innate drug delivery systems for cancer treatment: Recent advances, current obstacles, and challenges for clinical translation

Marco Pirisinu, Tin Chanh Pham, Daniel Xin Zhang, Tran Nguyen Hong, Lap Thi Nguyen, Minh T. N. Le

Summary: This article discusses the potential application of extracellular vesicles (EVs) as anticancer therapeutic agents. It highlights EVs' role in cancer immunotherapy and their advantages as delivery systems for anticancer agents. The article describes the biology of EVs, methods for their isolation, characterization, and functional analysis, as well as emerging challenges in EV imaging and drug loading strategies. It emphasizes the importance of standardized protocols and proper analytical approaches for rigorous and reproducible EV research.

SEMINARS IN CANCER BIOLOGY (2022)

Article Cell Biology

Covalent conjugation of extracellular vesicles with peptides and nanobodies for targeted therapeutic delivery

Tin Chanh Pham, Migara Kavishka Jayasinghe, Thach Tuan Pham, Yuqi Yang, Likun Wei, Waqas Muhammad Usman, Huan Chen, Marco Pirisinu, Jinhua Gong, Seongkyeol Kim, Boya Peng, Weixi Wang, Charlene Chan, Victor Ma, Nhung T. H. Nguyen, Dennis Kappei, Xuan-Hung Nguyen, William C. Cho, Jiahai Shi, Minh T. N. Le

Summary: The study presents a novel method for covalently conjugating EVs with targeting moieties using protein ligases, enabling specific delivery of therapeutic payloads to target cells without the need for genetic and chemical modifications. This approach shows promise for enhancing drug efficacy in cancer therapy by targeting specific receptors on cancer cells.

JOURNAL OF EXTRACELLULAR VESICLES (2021)

Article Biotechnology & Applied Microbiology

Red blood cell extracellular vesicles deliver therapeutic siRNAs to skeletal muscles for treatment of cancer cachexia

Boya Peng, Yuqi Yang, Zhiyuan Wu, Rachel Tan, Thach Tuan Pham, Eric Yew Meng Yeo, Marco Pirisinu, Migara Kavishka Jayasinghe, Tin Chanh Pham, Kun Liang, Ng Shyh-Chang, Minh T. N. Le

Summary: Cancer cachexia is a syndrome characterized by muscle loss, and inhibiting myostatin has shown promise in preserving muscle mass. However, existing methods of myostatin inhibition have had limited effectiveness and side effects. In this study, a novel method using red blood cell-derived extracellular vesicles to deliver Mstn siRNA to skeletal muscles was tested in a mouse model of cancer cachexia. The results showed that this delivery method was safe, non-inflammatory, and led to increased muscle growth and prevention of cachexia.

MOLECULAR THERAPY (2023)

Article Medicine, Research & Experimental

Surface-engineered extracellular vesicles for targeted delivery of therapeutic RNAs and peptides for cancer therapy

Migara Kavishka Jayasinghe, Marco Pirisinu, Yuqi Yang, Boya Peng, Thach Tuan Pham, Chang Yu Lee, Melissa Tan, Luyen Tien Vu, Xuan T. T. Dang, Tin Chanh Pham, Huan Chen, Anskar Y. H. Leung, William C. Cho, Jiahai Shi, Minh T. N. Le

Summary: The use of extracellular vesicles (EVs) as drug delivery vectors has gained attention due to their ability to efficiently deliver therapeutic payloads to diseased cells. Surface functionalization methods have been developed to enhance the stability and biocompatibility of EVs, allowing for targeted delivery to cancer cells and improved metastasis suppression. Extensive testing has shown that engineered EVs are biocompatible and safe for repeated dose treatment.

THERANOSTICS (2022)

Article Cell Biology

Red blood cell extracellular vesicles as robust carriers of RNA-based therapeutics

Chanh Tin Pham, Xin Zhang, Austin Lam, Minh T. N. Le

CELL STRESS (2018)

No Data Available