Journal of Cancer Immunology

Commentary Open Access

Expanding the Cancer Neoantigen Peptide Repertoire beyond In silico Tools

Amit Jain , Jackwee Lim

CD8+ cytotoxic T cells recognise and kill cancer cells that present immunogenic peptides bound to the cell surface major histocompatibility complex class I (MHC-I) molecules.

Review Article Open Access

SHP₂ Inhibition as a Promising Anti-cancer Therapy: Function in Tumor Cell Signaling and Immune Modulation

Jiawan Wang , Lindy Zhang , Christine A. Pratilas , Nicolas J. Llosa

The SHP2 phosphatase consists of one protein tyrosine phosphatase catalytic domain (PTP domain), two tandem Src homology 2 (SH2) domains (N-SH2 and C-SH2), and a C-terminal tail with two tyrosine phosphorylation sites (Tyr542 and Tyr580)

Commentary Open Access

Small-molecule Interferon Inducers for Cancer Immunotherapy Targeting Non-T cell-inflamed Tumors

Eunha Kim , Sanghee Lee

Since the discovery of escaping mechanism of tumor from negative immune regulation, the paradigm of drug discovery for anti-cancer agents has been dramatically shifted to cancer immunotherapy (e.g., dendritic cell therapy, CAR-T cell therapy, or antibody therapy) by stimulating patient’s immune system to treat cancer. 

Review Article Open Access

Emerging Strategies to Attack Polyploid Cancer Cells

Jing Zhang , Shenqiu Zhang , Qiong Shi , Dun Yang , Thaddeus D. Allen

While cells with a 2n complement of chromosomes are defined as diploid, cells that possess greater than 2n are referred to as polyploid.

Review Article Open Access

Mitochondria Autoimmunity and MNRR₁ in Breast Carcinogenesis: A Review

Félix Fernández Madrid , Lawrence I. Grossman , Siddhesh Aras

Recently, Aras et al. reported that MNRR1, a nuclear DNA (nDNA)-encoded mitochondrial antigen, promotes cancer cell migration and the development of metastasis as a proof of concept supporting the participation of mitochondrial autoimmunity in breast carcinogenesis.

Commentary Open Access

Inference of Clonal Copy Number Alterations from RNASequencing Data

Akdes Serin Harmanci , Arif O. Harmanci , Xiaobo Zhou

Tissues are composed of various types of interacting cells [1]. To understand the cellular organization and function in tissues, it is necessary to identify all of the different cell types and the locations of these different cell types within tissue structures.

Editorial Open Access

CTLA-4 and PD-L₁ or PD_-1 Pathways: Immune Checkpoint Inhibitors and Cancer Immunotherapy

Sachin Kumar Deshmukh

The immune system developed certain checks and balance to control or inhibit the reactivity against normal cells of the body. Uncontrolled immune responses to the non-self entities such as bacteria, viruses, parasites, or mutated self-antigens can cause an inflammatory reaction and autoimmune diseases.

Review Article Open Access

Leucocyte-Tumor Cell Hybridization Can Initiate Cancer Metastasis

John M. Pawelek , Zachary Grasmick , Eric Duvall , Greggory S. LaBerge

According to estimates from the International Agency for Research on Cancer, by the year 2030 there will be 22 million new cancer cases and 13 million deaths per year. The main reason for death from cancer is not the initial tumor but it’s metastasis to distant parts of the body, yet this process has remained poorly understood for quite some time.

Review Article Open Access

Salivary Protein Antigens for Breast Cancer Biomarkers

Imad Abrao Nemeir , Joseph Saab , Walid Hleihel , Abdelhamid Errachid , Nadia Zine

Breast Cancer is the most regularly diagnosed type of cancer in women in the world, making up on its own 25% of all cases, or nearly 2 million new cases in 2018, and 15% of all cancer related deaths, or around 626,700 deaths for that same year.

Editorial Open Access

Chimeric Antigen Receptor CAR NK Cells Emerging Immunotherapy for the Treatment of Cancer

Sachin Kumar Deshmukh

Although NK cells are recognized as effector lymphocytes of the innate immune system, they also regulate the adaptive immune response by releasing inflammatory cytokines and developing immunological memory. Unlike other lymphocytes such as T or B cells, NK cells do not express rearrangeable, antigen-specific receptors.