News Release 6-Apr-2021
Editor’s note: Some cancers including small cell lung cancer can be cured by simply taking some supplements and following a anti-cancer diet. Not every cancer can reap the same magnitude of benefits. But those who know a trick or two about alternative treatments eventually overcome their cancer. Many cancer patients not just survive, but also thrive after their cancer diagnosis. Cancer diagnosis to them is a turning point which forces them to reflect on their life and lifestyle. Once they get wiser and knows how to live a better life, the disease disappears naturally. We know a gentleman who was diagnosed with lung cancer in his early seventies, and in two years he got rid of all cancer masses by simply taking some supplements. After 19 or 20 years, he is still healthy and cancer free. Last time we talked was when he was 93 year old.
編者註：只需服用一些補充劑並遵循抗癌飲食，即可治愈包括小細胞肺癌在內的某些癌症。 並非每種癌症都能獲得同等的收益。 但是那些對替代療法一竅不通的人最終會克服他們的癌症。 許多癌症患者不僅可以生存，而且在診斷出癌症後也可以壯成長。 對他們的癌症診斷是一個轉折點，迫使他們反思自己的生活和生活方式。 一旦他們變得更聰明並且知道如何過上更好的生活，這種疾病就會自然消失。 我們認識一位紳士，他在70年代初被診斷出患有肺癌，兩年之內，他通過服用一些補充劑擺脫了所有癌症。 19 20年之後，他也很健康。 上一次我們談的是他93歲那年。
University of Cologne
Using samples of small cell lung tumours, a research team led by biologist Dr Silvia von Karstedt has discovered two new ways to induce tumour cell death. One of two subsets of tumour cells can be targeted by activating ferroptosis: iron-dependent cell death caused by oxidative stress. In the second subtype, oxidative stress – and hence cell death – can also be induced in a different way. Both types of cell death must be triggered simultaneously by drugs to kill the majority of the tumour mass. The results of the study have been published in Nature Communications.
Despite many advances in treatment, a diagnosis of small cell lung cancer means a particularly poor prognosis. In Germany, up to 8000 new cases of small cell lung cancer (SCLC) are diagnosed each year. At the time of diagnosis, cancer has already found many loopholes to escape the body’s immune system. ‘Traditional’ cell death mechanisms, such as regulated cell death by apoptosis, are usually already inactivated at this stage. That way, tumour cells can continue to divide and spread almost unperturbed.
A high cell division rate is characteristic of small cell lung cancer, which initially promises a good response to chemotherapy. ‘Unfortunately, in many cases the success of chemotherapy is short-lived because tumour cells rapidly develop resistance to therapy. In addition, a tumour consists not only of one, but of several cell types – the so-called subtypes – each of which uses unique strategies to escape lethal therapy,’ said von Karstedt, research group leader at the CECAD Cluster of Excellence for Aging Research, the Department of Translational Genomics at the University of Cologne and the Center for Molecular Medicine Cologne (CMMC). This is where her research comes in. The biologist explores which cell death mechanisms are already inactivated in cancer cells and which ones can still be targeted by therapies to kill the tumour.
The research team used patient samples taken at the time of diagnosis, thus depicting the treatment-naïve tumour. To find out which pathways of cell death are still available, the scientists compared gene activity between patient cells taken inside and outside the tumour. Signalling pathways important for traditional cell death mechanisms were already switched off inside the tumour at this early stage, before therapy. In contrast, genes important for the activation of iron-dependent cell death by oxidative damage (ferroptosis) were strongly activated in the cancer cells.
Put in simple terms, small cell lung cancer cells can be divided into two subtypes: neuroendocrine cells and non-neuroendocrine cells. In the neuroendocrine cell subtype, more genes are active which are otherwise typically found in nerve cells that produce hormones. Cells belonging to the other subtype do not have this property and are therefore grouped as non-neuroendocrine cells. ‘Several experiments showed that cells of the non-neuroendocrine type can be killed using buthionine sulfoximine, which induces ferroptosis. In cells belonging to the neuroendocrine subtype, we found that they protect themselves from oxidative stress – and thus cell death – by producing antioxidants. However, by adding the antioxidant inhibitor Auranofin, we were able to kill these cells as well,’ explains doctoral researcher Christina Bebber, the lead author of the paper.
Regarding a possible application of these findings to the therapy of small cell lung cancer, the biologists made an important observation: When targeting just one of the two pathways – i.e., either activating ferroptosis or inhibiting antioxidant production – in a tumour consisting of cells of both subtypes, cancer cells were able to evade the lethal therapy. They did so by adjusting their gene expression to switch to the subtype that could resist the respective single pathway-targeting treatment. ‘When we applied a combination therapy, we took away this route of escape. What is also special about the study is that we used drugs that have already been tested in extensive clinical trials or even approved for the treatment of other diseases,’ von Karstedt explained. Buthionine sulfoximine, which triggers ferroptosis, is already in clinical trials for cancer treatment. The gold salt Auranofin, which blocks the production of protective antioxidants in cancer cells, has been in use for decades to treat rheumatoid arthritis.
Future clinical studies using this combined therapy will clarify to what extent this targeted therapy option will improve the prognosis of small cell lung cancer patients.