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Research

Oct 10th, 2024
Why Do Employees Keep Their Ideas from Their Bosses?

TAU research reveals that 1 in 4 employees hide their inventions from their employers.

  • Management

A new study from the Coller School of Management at Tel Aviv University sheds light for the first time on an important issue in the business world: employees withholding their inventions from the companies they work for. Although the law and/or employment contracts typically grant organizations the rights to their employees’ inventions, invention withholding is quite common. It carries serious implications for businesses, especially in knowledge-intensive industries. The study reveals alarming data: one out of every four employees in commercial organizations has withheld an invention from their employer at least once. In many cases, this withholding is done deliberately, with the intent to use the invention after leaving the organization. The research was led by Dr. Sarit Erez, in collaboration with Prof. Yaniv Shani and Prof. Abraham Carmeli from the Coller School of Management at Tel Aviv University. The study was published in the prominent journal Academy of Management Perspectives.

 

Coller School of Management.

 

Dr. Erez explains: "Commercial organizations, particularly those in knowledge-intensive industries, encourage innovation among their employees, and their success largely depends on those employees coming up with groundbreaking inventions. To protect companies’ rights to these inventions, legal systems and standard employment contracts typically grant the employer ownership of inventions made by their employees, while requiring employees to disclose any invention they have come up with at work. This allows the employer to obtain patents and protect the invention. To increase employees’ motivation to disclose their inventions, many companies implement incentive systems, offering financial grants and/or recognition, such as badges of honor, to inventors. But at the end of the day, when an employee comes up with a new invention, they are faced with a behavioral dilemma: should they fulfill their legal obligation and disclose the invention to their employer, knowing they will lose ownership, or violate their obligation and hold on to the possibility of capitalizing on their invention outside the company? Indeed, it is a common scenario to see people leave one organization and either join another in the same field or even start their own company — often to develop an invention conceived in their previous workplace".

 

Video Credit: Dr. Sarit Erez.

 

 

Who Really Owns the Work You Create?

Dr. Erez continues: "These types of cases often end up in court, where an employer sues a former employee — or their new employer — alleging that they are using an invention that the employee conceived while working for them and that the patent rightfully belongs to the original employer. Having practiced law in the private sector for about 20 years, I often represented employees, employers, or employee organizations in disputes of this type. It became evident that the legal tools currently used to address this issue are not the most effective approach. I used to believe that management tools were designed to increase employees’ willingness to disclose their inventions and reduce their tendency to withhold them could be far more effective. But when I looked for academic research on this subject, I found only a handful, and even those focused mainly on the withholding of inventions in academia rather than in commercial organizations. It became clear to me that the issue of withholding inventions, which is so vital to the growth of knowledge-driven companies, had not yet been thoroughly explored in management strategy. With this study, we aimed to shed light on this important phenomenon and begin to address it from a business perspective".

 

For the study, the researchers distributed an anonymous online questionnaire, asking inventors to report whether they had ever withheld one or more inventions from their employers. Participants were also requested to describe the event, including its reasons and circumstances. A total of 199 valid responses were collected. Dr. Erez details the findings: "54 participants, or 27 percent of the respondents, reported withholding at least one invention from the organization in which they worked. Of these, 28 percent explicitly stated that they did so to develop the invention themselves after leaving the organization or bringing it as a sort of ‘dowry’ to their next employer. The others cited a variety of reasons, some psychological and some financial. These included an emotional attachment and sense of ownership over the invention as a personal creation; fear that someone else would take credit; conflict with their employer; lack of trust in management; dissatisfaction with pay; and the belief that they would not be adequately compensated for an invention that would profit the organization".

 

Changing the Work Culture

In the next phase, the researchers developed a unique and validated measurement scale, the first of its kind, to assess employees’ tendencies to either disclose or withhold inventions from their employers. The findings revealed that withholding or disclosing inventions are not simply opposite sides of the same behavior, but rather two fundamentally different behaviors: an employee might refrain from disclosing a certain invention for a variety of reasons (such as a heavy workload or the belief that the invention still requires development and is not ready to be disclosed). However, a deliberate and active decision to withhold an invention in order to prevent the transfer of ownership to the organization is a distinct behavior that may be influenced by completely different factors (for example, the employee’s feeling that they are poorly treated by the company regardless of the invention itself). Dr. Erez explains: “This distinction is extremely important for organizations seeking to address the problem. Actions taken by companies today, such as offering financial incentives or recognition to inventors, may encourage more disclosures to the organization. However, such measures may be less effective for employees who deliberately withhold a promising invention with the intention of using it further down the road, outside the organization”.

 

According to the researchers, this newly developed scale can serve as a foundation for further studies on the subject. Additionally, it can help employers build an effective innovation management strategy that minimizes the withholding of inventions within the organization.

 

Dr. Erez concludes: “In this study, we conducted an in-depth exploration of a widespread phenomenon that has long concerned legal professionals around the world, but so far has hardly been examined from a managerial perspective: employees in the business sector who withhold their inventions from the company that employs them. We urge researchers in academia to continue investigating this important topic, and call on employers to take notice: these behaviors exist, and it is crucial to address them. For our follow-up studies, we are developing management tools to help employers tackle the issue in all its complexity. We believe that with the right management strategies, it is possible to encourage disclosure and significantly reduce the withholding of inventions — preventing the need for legal battles down the line”.

Research

Oct 1st, 2024
Corals on Drugs: A Threat We Can't Ignore

10 different pharmaceuticals detected in corals in the Gulf of Eilat

  • Environment

Severe environmental contamination: A new study from Tel Aviv University and the Steinhardt Museum of Natural History detected traces of 10 common medications in coral samples collected from both shallow and deep sites in the Gulf of Eilat. Sulfamethoxazole, an antibiotic used for respiratory and urinary tract infections, was found in 93% of the sampled corals.

 

The alarming study was led by Prof. Noa Shenkar of TAU's School of Zoology, Faculty of Life Sciences and Steinhardt Museum of Natural History, and her PhD student Gal Navon, in collaboration with the Hydrochemistry laboratory led by Prof. Dror Avisar at TAU's Porter School of Environment and Earth Sciences. The results were published in the prestigious journal Environmental Pollution.

 

אלמוג אבן מסוג FAVITES

The stony coral species Favites (Photo Credit: Prof. Noa Shenkar).

 

"In this first-of-its-kind study, we conducted a large-scale investigation for detection of pharmaceuticals in corals", says Prof. Shenkar. "We sampled 96 reef-building stony corals representing two types, Acropora sp. and Favites sp., in shallow sites (5-12 meters) as well as deeper sites beyond the limits of recreational diving (30-40 meters). We were surprised to find an extensive presence of medications even in the deep-water corals - which usually escape contaminations affecting corals in shallower areas".

 

A Cocktail of Drugs Found in Coral Reefs

The researchers obtained a list of the most commonly used pharmaceuticals in Israel from Clalit Health Services. Testing for 18 of these compounds, they detected 10 of them in the coral samples. Not even a single sample, retrieved from either shallow or deep water, was found to be drug-free. The 10 pharmaceuticals found in the corals belonged to different categories: antibiotics, blood pressure medications, antiplatelet agents, calcium channel blockers, laxatives, proton pump inhibitors, statins and antidepressants.

 

"What does the presence of pharmaceuticals in corals actually mean? Clearly, the corals did not receive a prescription for antibiotics from their doctor", explains Prof. Shenkar. "These medications are taken by humans to affect a certain receptor or biological pathway, and they can also impact other organisms. Previous studies, conducted by both our lab and others, have revealed many examples of this negative impact: estrogen from birth control contraceptive pills induces female features in male fish, impairing reproduction in certain species; Prozac makes some crabs aggressive and reckless; and antidepressants damage the memory and learning abilities of squids. There is no reason to believe that corals should be immune to such effects. For instance, if our pharmaceuticals should disrupt the spawning synchrony of coral populations, it would take us a long time to notice the problem, and when we do, it might be too late".

 

פרופ' נועה שנקר וחברים ימיים

Prof. Noa Shenkar.

 

"Stony corals build coral reefs, and the types we studied are very common in the Gulf of Eilat", adds Gal Navon. "Coral reefs are a cornerstone of marine biodiversity. They provide food, shelter, and spawning sites to numerous species, and support the human fishing and tourism industries. Today this delicate ecosystem is under pressure as a result of climate change, pollution, and overfishing. The presence of pharmaceuticals in coral tissues adds another layer of concern, indicating that human activities even contaminate faraway marine environments".

 

"Clearly these medications save lives, and we have no intention of requesting people to reduce their use", says Prof. Shenkar. "However, we must develop new sewage treatment methods that can effectively handle pharmaceutical compounds. Also, each of us must dispose of old medications in ways that do not harm the environment. Ultimately these drugs come back to us. I know people who avoid medications, but when they eat a fish, they might unknowingly consume a 'cocktail' of drug residues absorbed by the fish from the marine environment".

Research

Sep 23rd, 2024
Could Cancer Vulnerabilities Be Hidden in Chromosome Changes?

TAU researchers uncover cancer weaknesses, paving the way for targeted treatments.

  • Medicine

Two complementary studies from the Faculty of Medical and Health Sciences at Tel Aviv University, in collaboration with the European Institute of Oncology in Milan, have extensively examined the characteristics of cells with an abnormal number of chromosomes - known as aneuploid cells - and raised findings that may advance new cancer treatments.

 

Targeting Aneuploid Cancer Cells

According to the researchers: "a significant portion of cancer cells are aneuploid, and this trait distinguishes them from healthy cells. Our work focuses on the vulnerabilities of aneuploid cells, with the aim of promoting new strategies for eliminating cancerous tumors".

 

The researchers: "In our studies, we found that aneuploidy increases the sensitivity of cancer cells to certain types of anticancer drugs".

 

The studies were led by Prof. Uri Ben-David and doctoral student Johanna Zerbib from the Department of Human Molecular Genetics and Biochemistry at the Faculty of Medical and Health Sciences at Tel Aviv University, in collaboration with Professor Stefano Santaguida and doctoral student Marica Rosaria Ippolito from the University of Milan in Italy, along with researchers from both laboratories. Additional contributors included research teams in Israel, Italy, the USA, and Germany. Two articles based on the research were published in the prestigious journals Cancer Discovery and Nature Communications.

 

Prof. Ben-David explains: "In the nucleus of a healthy human cell, there are 23 pairs of chromosomes - half from the father and half from the mother, totaling 46. One of the characteristics of cancer cells, which distinguishes them from healthy cells, is an abnormal number of chromosomes, resulting from improper cell division - a phenomenon known as aneuploidy. We believe that if we can identify specific vulnerabilities of aneuploid cells, we can promote new cancer treatments that target these weaknesses and do not harm healthy cells. About three years ago, we published a comprehensive study in the journal Nature, in which we classified approximately 2,000 malignant cells from various cancer types according to their level of aneuploidy, and examined how they respond to various existing treatments. In that study, we found new vulnerabilities in aneuploid cells. However, the study had a limitation: because the cells came from different types of cancer, it was difficult to isolate the impact of aneuploidy itself from the effect of other genetic differences between the tumors".

 

Consequently, the researchers chose to conduct a new study using human cell cultures that are all genetically identical (i.e., derived from the same individual). The researchers added a substance to the cultures that disrupts the separation of chromosomes, causing some of them to become aneuploid. Since the cells were genetically identical, the only difference between them after the procedure was the level of aneuploidy - i.e., the number of chromosomes. To thoroughly examine the effects of aneuploidy, the cells underwent various characterization processes: DNA and RNA sequencing, measuring the levels of all the proteins in the cell, assessing the response to 6,000 different drugs, as well as a process known as CRISPR screening - systematically impairing each gene in the genome to identify genes that are essential in the cells. The researchers noted: "In this way, an extensive and unique database of the characteristics of aneuploid cells was established, which can serve as a foundation for future studies, as well as for developing biological markers that predict cancer patients' responses to specific drugs and treatments".

 

 

How to Exploit Cell Vulnerabilities for Cancer Therapy?

As part of the comprehensive survey, a mechanism called MAPK (mitogen-activated protein kinase) was observed, which is especially crucial for repairing DNA damage in aneuploid cells. The study also showed that this mechanism is relevant for various types of aneuploid cells—among them cancer cells in cultures and in human tumors. Prof. Ben-David: "We found that aneuploid cancer cells increase the activity of DNA repair mechanisms due to the large amount of DNA damage present; and we discovered a mechanism that could allow us to exploit this characteristic to target these cancer cells".

 

To test their hypothesis, the researchers disrupted the MAPK pathway in the cells and then examined their sensitivity to chemotherapy. The findings were promising: aneuploid cells in which this mechanism was disrupted were much more sensitive to chemotherapy (which causes DNA damage) compared to cells with a normal number of chromosomes. The researchers then sought to determine whether there is a correlation between this pathway and the clinical response of cancer patients to chemotherapy treatments. For this purpose, they relied on data from clinical treatments and experiments where human tumors were implanted in mice, and the results were clear: the higher the activity of the pathway in the aneuploid tumors, the greater their resistance to chemotherapy.

 

The comprehensive characterization of aneuploid cells also revealed another significant finding: these cells, which contain more chromosomes than normal cells, also necessarily include a larger amount of DNA, leading to excess production of RNA and proteins. The cell, seeking to compensate for this overproduction, attempts to silence and degrade excess RNA and proteins.

 

Paving the Way for Future Treatments

Johanna Zerbib noted: "Here we found another vulnerability of aneuploid cells, based on our hypothesis that these cells are more sensitive to existing drugs that inhibit protein degradation. To validate this hypothesis, we exposed cell cultures to such drugs and analyzed clinical data from patients treated with a drug that inhibits protein degradation in the cells. The findings supported the hypothesis - that aneuploidy increases the sensitivity of cancer cells to these drugs".

 

Prof. Ben-David concluded: "In our research, we identified two significant vulnerabilities characterizing aneuploid cells - cells with chromosomal changes, commonly found in cancer cells. The first is a mechanism essential for repairing DNA damage, where impairment significantly increases the sensitivity of aneuploid cells to chemotherapy; the second is the increased degradation of excess RNA and proteins, which can be targeted, among other things, with inhibitors that are already in clinical use. We also created an extensive database of characteristics of aneuploid cells that can serve to predict cancer patients' responses to various drugs and treatments. We believe that our research findings will benefit many researchers, oncologists, and patients in the years to come".

 

Research

Sep 17th, 2024
Spotting Parkinson’s Early: A New TAU Breakthrough

Researchers have developed revolutionary tech to detect Parkinson’s up to 20 years before symptoms appear.

  • Medicine

Researchers at Tel Aviv University cooperated with three major Israeli medical centers to develop a new method for detecting protein aggregation in cells – a hallmark of Parkinson's disease. The technology can enable diagnosis up to 20 years before the first motor symptoms appear, facilitating treatment or even prevention of the severe disease which is currently incurable. The novel approach is based on super-resolution microscopy combined with computational analysis, allowing for precise mapping of the aggregates' molecules and structures. The researchers: "Our method can be used to identify early signs and enable preventive treatment in young people at risk for developing Parkinson's later on in their lives. In the future, the technology may also be adapted for early diagnosis of other neurodegenerative diseases, including Alzheimer's".

 

The study was conducted by researchers from the School of Neurobiology, Biochemistry & Biophysics at the Wise Faculty of Life Sciences, the Sagol School of Neuroscience and the Faculty of Medical and Health Sciences at Tel Aviv University, led by Prof. Uri Ashery and PhD candidate Ofir Sade. The research was supported in part by TAU’s Aufzien Family Center for the Prevention and Treatment of Parkinson's Disease.

 

Other participants included: Prof. Anat Mirelman, Prof. Avner Thaler, Prof. Nir Giladi, Prof. Roy Alcalay, Prof. Sharon Hassin, Prof. Nirit Lev, Dr. Irit Gottfried, Dr. Dana Bar-On, Dr. Meir Kestenbaum, Dr. Saar Anis, Dr. Shimon Shahar, Daphna Fischel, Dr. Noa Barak-Broner, Shir Halevi, and Dr. Aviv Gour – all from Tel Aviv University, with some also affiliated with the Tel Aviv Sourasky (Ichilov), Sheba, or Meir Medical Centers. Researchers from Germany and the USA also contributed to the study. The paper was published in Frontiers in Molecular Neuroscience.

 

 

Spotting Parkinson’s Before Symptoms Appear

Prof. Ashery: "Parkinson's disease is the second most prevalent neurodegenerative disease in the world after Alzheimer's - with about 8.5 million people with Parkinson's living worldwide today, and 1,200 new sufferers diagnosed annually in Israel. The debilitating disease is characterized by the destruction of dopaminergic (dopamine-producing) neurons in the brain's Substantia Nigra area. Today, diagnosis of Parkinson's disease is based mainly on clinical symptoms such as tremors or gait dysfunctions, alongside relevant questionnaires. However, these symptoms usually appear at a relatively advanced stage of the disease, when over 50% and up to 80% of the dopaminergic neurons in the Substantia Nigra are already dead. Consequently, available treatments are quite limited in their effect and usually address only motor problems. In this study, we began to develop a research tool to enable diagnosis of Parkinson's at a much earlier stage, when it is still treatable, and deterioration can be prevented".

 

Ofir Sade: "One known feature of Parkinson's is cell death resulting from aggregates of the alpha-synuclein protein. The protein begins to aggregate about 15 years before symptoms appear, and cells begin to die 5-10 years before diagnosis is possible with the means available today. This means that we have an extensive time window of up to 20 years for diagnosis and prevention before symptoms appear. If we can identify the process at an early stage, in people who are 30, 40, or 50 years old, we may be able to prevent further protein aggregation and cell death". Past studies have shown that alpha-synuclein aggregates form in other parts of the body as well, such as the skin and digestive system. In the current work, the researchers examined skin biopsies from 7 people with and 7 without Parkinson's disease, received from the Sheba, Ichilov, and Meir Medical Centers. 

 

She continues: "We examined the samples under a unique microscope, applying an innovative technique called super-resolution imaging, combined with advanced computational analysis - enabling us to map the aggregates and distribution of alpha-synuclein molecules.  As expected, we found more protein aggregates in people with Parkinson's compared to people without the disease. We also identified damage to nerve cells in the skin, in areas with a large concentration of the pathological protein".

 

 

Parkinson’s Detection Boosted by AI

With proof of concept obtained through the study, the researchers now plan to expand their work, supported by the Michael J. Fox Foundation for Parkinson's Research. In the next phase, they will increase the number of samples to 90 - 45 from healthy subjects and 45 from people without Parkinson's disease - to identify differences between the two groups. Ofir Sade: "We intend to pinpoint the exact juncture at which a normal quantity of proteins turns into a pathological aggregate. In addition, we will collaborate with Prof. Lior Wolf of TAU's Blavatnik School of Computer Science to develop a machine learning algorithm that will identify correlations between the results of motor and cognitive tests and our findings under the microscope. Using this algorithm, we will be able to predict the future development and severity of various pathologies".

 

Prof. Ashery: "In this study, we identified differences between tissues taken from people with and without Parkinson's disease, using super-resolution microscopy and computational analysis. In future studies, we will increase the number of samples and develop a machine-learning algorithm to spot relatively young individuals at risk for Parkinson's. Our main target population is relatives of Parkinson's patients who carry mutations that increase the risk for the disease. Specifically, we emphasize two mutations known to be widespread among Ashkenazi Jews. A clinical trial is already underway to test a drug expected to hinder the formation of the aggregates that cause Parkinson's disease. We hope that in the coming years, it will be possible to offer preventive treatments while tracking the effects of medications under the microscope. It is important to note that the method we've developed can also be suitable for early diagnosis of other neurodegenerative diseases associated with protein aggregates in neurons, including Alzheimer's".

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