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Enhancing ADCs to Target Diseased Cells and Deliver Payloads

Published on 04th February

Insulin-like growth factor or IGF is a natural growth hormone, which plays an important role in normal growth and development. Six soluble insulin-like growth factor-binding proteins or IGFBPs and IGFBP proteases regulate its actions. These binding proteins bind to Insulin-like growth factor with high affinity and specificity.[1]

Based on their current level of understanding of the mechanisms of action, scientists have shown that these IGFBPs are involved actions beyond their endocrine role in IGF transport. In the pericellular and intracellular compartments, for example, IGFBPs are instrumental in the regulation of cell growth and survival.

IGF and Cancer
Over the las decade, IGF has gained tremendous interest because it plays an important role in cancer. Conventional chemotherapy for the treatment of patients with cancer has limited specificity for cancer cells. In these cases, high doses of systemic chemotherapy used to treat patients have limited success and these patients experience significant side effects.

With the shift towards targeted therapies, a number of strategies have been exploited to target tumors directly. The most common of these strategies involves engineered antibodies or antibody fragments. The increased interest in IFG and cancer and this drive to targeted therapies, has resulted in strategies targeting various components of the IGF system. [2]

Insulin-like growth factor-1 receptor or IGF-1R activation is involved in cell regulation, survival and proliferation. In advanced cancers IGF-IRs are frequently genetically altered involving mutation, chromosomal translocation, abnormal stimulation, and loss of genomic imprinting. High levels of IGF-1 have been reported in several cases of breast and prostate cancers.[1][2]

Insulin-like growth factor-binding protein-3
Insulin-like growth factor-binding protein-3 or IGFBP‐3, first isolated, characterized, and quantitated in human plasma, in 1986, is the main IGF transport protein in the bloodstream directly influencing IGF action. [3][4] Via independent mechanisms involving interactions with plasma, extracellular matrices and cell surface molecules, conditional proteolysis, cellular uptake, and nuclear transport, IGFBP-3 also modulates IGF actions indirectly.[5]

IGFBP-3, which in plasma is known to participate in high-affinity interactions with the iron- binding proteins lactoferrin and transferrin, has been implicated with a variety of proteins or signaling cascades critical to cell cycle control and apoptosis.

Antiproliferative and proapoptotic effects of IGFBP-3, independent from IGF/IGF-IR, contribute to improving the pathophysiology of a variety of human diseases, such as cancer, as well as diabetes, and malnutrition.[6][7][8]

Metal-binding transporter domain
The amino acid metal-binding transporter domain or MBD derived from IGFBP‐3 selectively targets cancer cells. In a number of studies scientists have demonstrated that MBD-tagged anti-cancer peptides can have cytotoxic effects on a broad range of human cancer cell lines. In one of these studies, researchers investigated the discriminant validity of the molecules as potential cotherapeutic agents. By comparing their cytotoxicity to cancer cell lines versus normal human cell counterparts, the researchers demonstrated synergies between these molecules and marginally cytotoxic levels of 5-fluorouracil.[6]

Biodistribution data from in-vivo experiments in normal mice and rats further confirmed that MBD-tagged molecules preferentially localize to specific tissues including the kidney and pancreas and significantly reduced splenomegaly and bone marrow cancer cell burden in diseased animals. This suggests that MBD-tagged molecules can be used as highly selective chemosensitizers in the treatment of hematological and disseminated malignancies.

Functionalizing MBD
To enhance the ability of antibody-drug conjugates to target and deliver payloads directly to tumor cells, Goodwin Biotechnology, Inc., a biological Contract Manufacturing Organization or CMO (Plantation, FL) that specializes in Mammalian Cell Culture expression systems and Bioconjugation technologies, and Transporin, Inc. (Sunnyvale, CA), a Silicon Valley R & D company with full ownership of IP rights to a broad array of life science technologies, have agreed to collaborate on exploring and functionalizing Transporin’s proprietary metalbinding domain transporter technology in the development of antibody and peptide-based biopharmaceutical drugs.

Under the terms of the agreement Goodwin Biotechnology has been granted a worldwide, exclusive license to utilize the proprietary metalbinding domain of human insulin‐like growth factor binding protein‐3 conjugated to monoclonal antibodies or antibody fusion proteins, and perform process development and manufacturing services using such conjugates for research, evaluation, and clinical trial purposes.

Significant development
“This is a significant milestone for our company,” said Karl Pinto, CEO of Goodwin Biotechnology (Photo 1). “We have been committed to investing in and advancing the field of Bioconjugation for nearly 15 years, and this collaboration enables us to offer our clients a proprietary, enabling technology that promises to enhance the targeting ability of our clients’ antibodies, then enhance the ability for the payload to enter the target cell where it can do its job. This unique technology is designed to enhance the therapeutic ratio of efficacy while minimizing side effects and it may also reduce the cost of therapy—All of which have a positive impact on the quality of care for patients and their families.”

Proprietary peptides
“Transporin has developed a transporter module consisting of approximately 20 amino acids based on the metal‐binding domain of IGF‐binding proteins, which form part of a new generation of proprietary peptides,” said Desmond Mascarenhas, PhD, CEO of Transporin (Photo 2).

“When covalently attached to other peptides, large proteins or small nucleic acids, the MBD‐transporter can deliver these biomolecules intracellularly, differentiating between normal cells and cells under stress, and targeting the latter. Possible targets include many types of cancer, metabolic disease as well as autoimmune conditions. The MBD‐peptide complex rapidly transports its cargo into cytoplasmic and nuclear compartments of targeted cells.”

“When augmenting Goodwin Biotechnology’s expertise in Bioconjugation with our proprietary MBD peptide technology, the potential value of the resultant conjugate is increased multi‐fold,” Mascarenhas continued. “There are a number of applications that can be explored. For example, the MBD amino acid sequence can be incorporated as a linker to bind to a functional monoclonal antibody to generate an antibody‐linker‐drug conjugate. Another option is that the MBD peptide sequence can be genetically incorporated into the DNA sequence of a specific product to develop a unique cell line.”

Great potential
Further, when linking a monoclonal antibody to a radioactive metal, the MBD peptide sequence can be used as an excipient to bind the metal and possibly shield the radioisotope to protect healthy cells while the complex is in circulation while and enhancing the ability of the complex to target diseased cells via a non‐covalent interaction that doesn’t require a significant drug change.

The ability of the MBD amino acid sequence to bind to metals, specifically nickel, cobalt, zinc, iron and possibly other metals (including radioisotopes) may also help enhance the purification process for difficult‐to‐purify proteins using metal‐affinity columns.[5] The resultant MBD‐antibody- conjugatet can be used for diagnostic purposes, for monitoring diseases and/or as a therapeutic modality.

Unmet needs require a new approach
The potential value of the MBD‐peptide technology can best be appreciated when put in perspective. While modern medicine has made significant strides in the treatment of a large number of human disease conditions, including cancer, a number of diseases require advancements to improve detection, monitoring, and treatment.

Monoclonal antibodies (mAbs) conjugated with a payload such as a drug or radioisotope are showing some promise based on their ability to target diseased cells. However, based on the complexity of the antibody:linker:payload conjugate, premature cleavage of the payload from the conjugate, inability of the conjugate to breach the cell wall, binding to non‐target sites and/or getting eliminated from the body prematurely, some researchers suggest that greater than 95% of the administered dose never reaches the intracellular target.[8]

To counter this problem, higher drug doses are needed. However, higher drug doses increase the cost of therapy and the potential adverse effect profile. Fortunately, the possibility of improving the selectivity of therapy for a number of diseases can be enhanced by the use of targeting agents.

Stress: acute and chronic conditions
Diseased cells in chronic conditions such as arthritis, osteoporosis, atherosclerosis and cardiovascular diseases and autoimmune diseases are now increasingly being viewed as subject to inflammatory and oxidative stress.  As such, these cells express stress-related molecules, which are recognized by the MBD-trasporter sequence [12].  A number of cancers, especially breast, prostate, colon, ovarian, pancreatic, gastric and lung, express stress-related molecules as a survival strategy.  However, current treatments do not make use of this unique characteristic for targeting cancer cells.  Systemic damage from catastrophic stress, such as severe burn injury, also up-regulates neuro-immune stress mechanisms. [9]

The MBD peptide sequence can enhance the ability of the mAb to target diseased cells and improve targeting specificity an estimated 3x to 10x fold by binding to the cell surface transferrin receptor and integrin beta‐3. Hence, it can help reduce the off target effects of the drug and increase the speed of the agent to the target.[12]

The MBD peptide carrier also provides active transport into the target cell. MBD uptake correlates with the expression of genes associated with cellular stress‐coping mechanisms commonly up‐regulated in cancer (nuclear factor‐kappaB and HSP‐70B), for example. Once inside the cell, their payload can modify the disease process. For example, an MBD-linked inhibitor of Rictor complex, Nephrilin™ (Transporin, Inc), a novel intervention for disease processes triggered by stress, is currently in preclinical development for the treatment of metabolic disease and severe burns [9,10,12,13].

Further research in the possible therapeutic uses of the MBD transporter is expected to enhance the ability of antibody-drug conjugates to target diseased cells and deliver payloads.


Featured image: Image of a the radioisotope. Image Courtesy: Ekaterina (Kate) Dadachova, PhD and Arturo Casadevall, MD, PhD.  Image was originally published in Einstein’s dynamic duo of the decade. Einstein. 2010; Summer / Fall: 38-45.

Photo 1: Karl Pinto, CEO of Goodwin Biotechnology, is an entrepreneurial, seasoned executive whose career spans over 21 years in executive management and international business development in the USA and Asia.  He has been on the board of Goodwin since 2004 and was its Executive Chairman between 2004 and 2009. Karl earned an Engineering degree at the Manipal Institute of Technology and an MBA in Marketing & Finance from the University of Bombay. Photo Courtesy: Goodwin Biotechnology, Inc

Photo 2:  Desmond Mascarenhas, Ph.D, Chief Executive, Transporin, Inc. Mascarenhas owns three decades of experience in the technological innovation industries. He has established a successful track record as an entrepreneur, founding and operating ten corporate enterprises over the past eighteen years. Bioexpertise, Inc., a physician education company he founded in 2000 was recognized as an innovation leader in its field. Its clients included 12 of the 15 largest pharmaceutical companies. Mascarenhas has authored 30+ US patents and published dozens of peer-reviewed research papers. He holds a doctorate from Oxford University (which he attended as a Rhodes Scholar) and was a Post-doctorate Fellow at Stanford University. Photo Courtesy: Transporin, Inc.

Last Editorial Review: February 4, 2015

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